nsv4373339

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:53
Validation:Not tested
Clinical Assertions: No
Region Size:23,708

Publication(s):Zarrei et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 512 SVs from 43 studies. See in: genome view

Remapped(Score: Perfect):151,530,062-151,553,769

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4373339	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nsv4373339	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	150,698,534	150,722,241

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15613334	copy number loss	1-0696-004	SNP array	Genotyping	16
nssv15613423	copy number loss	1-0678-003	SNP array	Genotyping	18
nssv15614615	copy number loss	1-0733-003	SNP array	Genotyping	19
nssv15616019	copy number loss	1-0139-004	SNP array	Genotyping	15
nssv15617378	copy number loss	1-0842-003	SNP array	Genotyping	22
nssv15620107	copy number loss	1-0939-003	SNP array	Genotyping	26
nssv15627679	copy number loss	1-0533-002	SNP array	Genotyping	19
nssv15628075	copy number loss	1-0059-002	SNP array	Genotyping	19
nssv15629021	copy number loss	1-0546-004	SNP array	Genotyping	27
nssv15631590	copy number loss	1-1074-003	SNP array	Genotyping	17
nssv15633299	copy number loss	11-0017-003	SNP array	Genotyping	14
nssv15635254	copy number loss	11-0027-003	SNP array	Genotyping	17
nssv15638997	copy number loss	14-0243-003	SNP array	Genotyping	27
nssv15640043	copy number loss	14-0261-003	SNP array	Genotyping	11
nssv15640450	copy number loss	14-0286-003	SNP array	Genotyping	22
nssv15641077	copy number loss	14-0382-003	SNP array	Genotyping	22
nssv15642827	copy number loss	14-0385-003	SNP array	Genotyping	21
nssv15643238	copy number loss	14-0362-001	SNP array	Genotyping	18
nssv15644692	copy number loss	16-1000-003	SNP array	Genotyping	23
nssv15646046	copy number loss	16-1011-004	SNP array	Genotyping	17
nssv15653814	copy number loss	2-1567-003	SNP array	Genotyping	20
nssv15657016	copy number loss	3-0706-000	SNP array	Genotyping	22
nssv15657281	copy number loss	3-0345-001	SNP array	Genotyping	17
nssv15659094	copy number loss	4-0061-003	SNP array	Genotyping	28
nssv15659133	copy number loss	4-0065-001	SNP array	Genotyping	19
nssv15660436	copy number loss	4-0075-003	SNP array	Genotyping	24
nssv15662069	copy number loss	5-0084-002	SNP array	Genotyping	18
nssv15666829	copy number loss	7-0112-003	SNP array	Genotyping	26
nssv15667974	copy number loss	7-0161-003	SNP array	Genotyping	27
nssv15668049	copy number loss	7-0164-003	SNP array	Genotyping	22
nssv15670896	copy number loss	7-0284-003	SNP array	Genotyping	28
nssv15671724	copy number loss	9-0005-002	SNP array	Genotyping	18
nssv15673711	copy number loss	227574	SNP array	Genotyping	22
nssv15674743	copy number loss	205650	SNP array	Genotyping	20
nssv15676917	copy number loss	183433	SNP array	Genotyping	27
nssv15680144	copy number loss	227843	SNP array	Genotyping	15
nssv15680455	copy number loss	193296	SNP array	Genotyping	22
nssv15680496	copy number loss	193290	SNP array	Genotyping	25
nssv15683353	copy number loss	OCD106-1607(313)	SNP array	Genotyping	23
nssv15683925	copy number loss	OCD137-0625-2972-1	SNP array	Genotyping	20
nssv15684330	copy number loss	OCD1137-7286	SNP array	Genotyping	20
nssv15684691	copy number loss	OCD153-MD-1368(189719)	SNP array	Genotyping	18
nssv15684710	copy number loss	OCD153-WD-140-1366	SNP array	Genotyping	19
nssv15688990	copy number loss	227580	SNP array	Genotyping	22
nssv15689372	copy number loss	OCD100-1571	SNP array	Genotyping	23
nssv15689715	copy number loss	OCD1122-896053	SNP array	Genotyping	22
nssv15691151	copy number loss	OCD27-S_896533	SNP array	Genotyping	23
nssv15691408	copy number loss	OCD42-S_0625-2765-1	SNP array	Genotyping	28
nssv15693934	copy number loss	OCD97-1399-2	SNP array	Genotyping	15
nssv15696941	copy number loss	118261	SNP array	Genotyping	23
nssv15698605	copy number loss	158447	SNP array	Genotyping	24
nssv15699926	copy number loss	79158	SNP array	Genotyping	20
nssv15702901	copy number loss	202163	SNP array	Genotyping	29

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15613334	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15613423	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15614615	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15616019	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15617378	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15620107	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15627679	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15628075	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15629021	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15631590	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15633299	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15635254	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15638997	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15640043	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15640450	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15641077	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15642827	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15643238	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15644692	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15646046	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15653814	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15657016	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15657281	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15659094	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15659133	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15660436	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15662069	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15666829	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15667974	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15668049	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15670896	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15671724	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15673711	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15674743	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15676917	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15680144	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15680455	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15680496	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15683353	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15683925	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15684330	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15684691	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15684710	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15688990	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15689372	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15689715	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15691151	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15691408	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15693934	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15696941	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15698605	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15699926	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15702901	Remapped	Perfect	NC_000023.11:g.(?_ 151530062)_(151553 769_?)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	151,530,062	151,553,769
nssv15613334	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15613423	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15614615	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15616019	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15617378	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15620107	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15627679	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15628075	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15629021	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15631590	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15633299	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15635254	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15638997	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15640043	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15640450	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15641077	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15642827	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15643238	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15644692	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15646046	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15653814	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15657016	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15657281	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15659094	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15659133	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15660436	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15662069	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15666829	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15667974	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15668049	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15670896	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15671724	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15673711	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15674743	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15676917	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15680144	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15680455	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15680496	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15683353	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15683925	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15684330	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15684691	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15684710	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15688990	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15689372	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15689715	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241
nssv15691151	Submitted genomic		NC_000023.10:g.(?_ 150698534)_(150722 241_?)del	GRCh37 (hg19)		NC_000023.10	ChrX	150,698,534	150,722,241

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dbVar

Database of genomic structural variation

nsv4373339

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Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant