nsv4383855

Organism: Homo sapiens

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

Variant Calls:44
Validation:Not tested
Clinical Assertions: No
Region Size:53,748

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: 596 SVs from 56 studies. See in: genome view

Remapped(Score: Good):104,004,609-104,058,356

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4383855	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nsv4383855	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	103,259,181	103,312,921

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15614596	copy number gain	1-0732-003	SNP array	Genotyping	21
nssv15615746	copy number gain	1-0780-003	SNP array	Genotyping	21
nssv15615768	copy number gain	1-0780-004	SNP array	Genotyping	21
nssv15617765	copy number gain	1-0850-003	SNP array	Genotyping	17
nssv15618252	copy number gain	1-0860-003	SNP array	Genotyping	31
nssv15618623	copy number gain	1-0870-003	SNP array	Genotyping	15
nssv15621593	copy number gain	1-1005-004	SNP array	Genotyping	21
nssv15622084	copy number gain	1-1047-003	SNP array	Genotyping	18
nssv15623087	copy number gain	1-1052-003	SNP array	Genotyping	23
nssv15624952	copy number gain	1-0045-004	SNP array	Genotyping	27
nssv15633284	copy number gain	11-0016-004	SNP array	Genotyping	19
nssv15633600	copy number gain	11-0030-003	SNP array	Genotyping	15
nssv15636919	copy number gain	14-0017-003	SNP array	Genotyping	18
nssv15637194	copy number gain	12-4855-003	SNP array	Genotyping	27
nssv15640020	copy number gain	14-0258-004	SNP array	Genotyping	14
nssv15641613	copy number gain	14-0238-004	SNP array	Genotyping	23
nssv15642881	copy number gain	15-1119-001	SNP array	Genotyping	26
nssv15644478	copy number gain	16-1018-003	SNP array	Genotyping	19
nssv15644644	copy number gain	16-1000-001	SNP array	Genotyping	21
nssv15645603	copy number gain	16-1018-004	SNP array	Genotyping	22
nssv15651427	copy number gain	2-1433-003	SNP array	Genotyping	14
nssv15651441	copy number gain	2-1433-004	SNP array	Genotyping	13
nssv15652076	copy number gain	2-1512-003	SNP array	Genotyping	19
nssv15654771	copy number gain	3-0261-000	SNP array	Genotyping	82
nssv15655120	copy number gain	2-1690-002	SNP array	Genotyping	24
nssv15655715	copy number gain	2-1703-003	SNP array	Genotyping	16
nssv15656088	copy number gain	3-0632-000	SNP array	Genotyping	28
nssv15656176	copy number gain	3-0703-000	SNP array	Genotyping	28
nssv15656518	copy number gain	2-1753-003	SNP array	Genotyping	19
nssv15657090	copy number gain	3-0778-000	SNP array	Genotyping	23
nssv15658515	copy number gain	4-0046-003	SNP array	Genotyping	23
nssv15660679	copy number gain	5-0037-003	SNP array	Genotyping	18
nssv15665239	copy number gain	6-0475-003	SNP array	Genotyping	23
nssv15665980	copy number gain	5-0028-003	SNP array	Genotyping	19
nssv15671405	copy number gain	7-0283-003	SNP array	Genotyping	14
nssv15671448	copy number gain	7-0303-003	SNP array	Genotyping	15
nssv15673582	copy number gain	9-0042-003	SNP array	Genotyping	23
nssv15677073	copy number gain	218110	SNP array	Genotyping	20
nssv15677094	copy number gain	218109	SNP array	Genotyping	21
nssv15677659	copy number gain	218118	SNP array	Genotyping	29
nssv15678058	copy number gain	241609	SNP array	Genotyping	24
nssv15680633	copy number gain	214104	SNP array	Genotyping	18
nssv15681305	copy number gain	13AG1244	SNP array	Genotyping	30
nssv15681937	copy number gain	211604	SNP array	Genotyping	13

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15614596	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15615746	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15615768	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15617765	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15618252	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15618623	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15621593	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15622084	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15623087	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15624952	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15633284	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15633600	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15636919	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15637194	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15640020	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15641613	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15642881	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15644478	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15644644	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15645603	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15651427	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15651441	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15652076	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15654771	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15655120	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15655715	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15656088	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15656176	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15656518	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15657090	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15658515	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15660679	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15665239	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15665980	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15671405	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15671448	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15673582	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15677073	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15677094	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15677659	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15678058	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15680633	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15681305	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15681937	Remapped	Good	NC_000023.11:g.(?_ 104004609)_(104058 356_?)dup	GRCh38.p12	First Pass	NC_000023.11	ChrX	104,004,609	104,058,356
nssv15614596	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15615746	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15615768	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15617765	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15618252	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15618623	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15621593	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15622084	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15623087	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15624952	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15633284	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15633600	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15636919	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15637194	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15640020	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15641613	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15642881	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15644478	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15644644	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15645603	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15651427	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15651441	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15652076	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15654771	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15655120	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15655715	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15656088	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15656176	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15656518	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15657090	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15658515	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15660679	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15665239	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15665980	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15671405	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15671448	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15673582	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15677073	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15677094	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15677659	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15678058	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15680633	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15681305	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921
nssv15681937	Submitted genomic		NC_000023.10:g.(?_ 103259181)_(103312 921_?)dup	GRCh37 (hg19)		NC_000023.10	ChrX	103,259,181	103,312,921

dbVar

Database of genomic structural variation

nsv4383855

Links to Other Resources

Genome View

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