nsv4376485

Organism: Homo sapiens

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

Variant Calls:50
Validation:Not tested
Clinical Assertions: No
Region Size:60,328

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: 565 SVs from 81 studies. See in: genome view

Remapped(Score: Perfect):173,522,063-173,582,390

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4376485	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nsv4376485	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000003.11	Chr3	173,239,853	173,300,180

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15613498	copy number gain	1-0685-003	SNP array	Genotyping	20
nssv15618212	copy number gain	1-0859-003	SNP array	Genotyping	17
nssv15622008	copy number gain	1-0191-004	SNP array	Genotyping	22
nssv15623562	copy number gain	1-0269-002	SNP array	Genotyping	29
nssv15623583	copy number gain	1-0269-003	SNP array	Genotyping	20
nssv15626063	copy number gain	1-0409-003	SNP array	Genotyping	21
nssv15627724	copy number gain	1-0534-002	SNP array	Genotyping	23
nssv15628979	copy number gain	1-0546-002	SNP array	Genotyping	22
nssv15631725	copy number gain	10-0014-002	SNP array	Genotyping	26
nssv15634324	copy number gain	11-0007-003	SNP array	Genotyping	16
nssv15634460	copy number gain	11-0041-004	SNP array	Genotyping	16
nssv15635257	copy number gain	12-4139-003	SNP array	Genotyping	27
nssv15636198	copy number gain	13-0132-001	SNP array	Genotyping	17
nssv15636608	copy number gain	13-0135-002	SNP array	Genotyping	31
nssv15637134	copy number gain	12-4855-001	SNP array	Genotyping	22
nssv15637999	copy number gain	14-0062-001	SNP array	Genotyping	19
nssv15640175	copy number gain	14-0119-002	SNP array	Genotyping	22
nssv15641672	copy number gain	14-0243-003	SNP array	Genotyping	27
nssv15642083	copy number gain	15-1130-002	SNP array	Genotyping	17
nssv15642102	copy number gain	15-1130-003	SNP array	Genotyping	18
nssv15642820	copy number gain	14-0385-003	SNP array	Genotyping	21
nssv15649624	copy number gain	2-1467-003	SNP array	Genotyping	16
nssv15652458	copy number gain	2-1519-003	SNP array	Genotyping	17
nssv15653110	copy number gain	2-1623-001	SNP array	Genotyping	29
nssv15653757	copy number gain	2-1629-003	SNP array	Genotyping	16
nssv15653874	copy number gain	2-1598-003	SNP array	Genotyping	18
nssv15658061	copy number gain	3-0538-000	SNP array	Genotyping	23
nssv15659547	copy number gain	3-0772-000	SNP array	Genotyping	17
nssv15664652	copy number gain	4-0078-002	SNP array	Genotyping	34
nssv15664693	copy number gain	4-0078-004	SNP array	Genotyping	18
nssv15665859	copy number gain	7-0100-003	SNP array	Genotyping	16
nssv15669639	copy number gain	7-0276-003	SNP array	Genotyping	15
nssv15669887	copy number gain	7-0253-005	SNP array	Genotyping	19
nssv15670148	copy number gain	7-0258-004	SNP array	Genotyping	30
nssv15670736	copy number gain	7-0242-003	SNP array	Genotyping	18
nssv15674537	copy number gain	9-0045-002	SNP array	Genotyping	22
nssv15677496	copy number gain	213161	SNP array	Genotyping	18
nssv15680408	copy number gain	239189S	SNP array	Genotyping	27
nssv15680506	copy number gain	213165	SNP array	Genotyping	24
nssv15680558	copy number gain	214100	SNP array	Genotyping	14
nssv15681177	copy number gain	239188S	SNP array	Genotyping	27
nssv15681384	copy number gain	OCD103-1583	SNP array	Genotyping	24
nssv15681701	copy number gain	244411S	SNP array	Genotyping	30
nssv15684321	copy number gain	OCD1137-7286	SNP array	Genotyping	20
nssv15688560	copy number gain	OCD34-S_896672	SNP array	Genotyping	20
nssv15690616	copy number gain	OCD154-896622	SNP array	Genotyping	20
nssv15694631	copy number gain	203864	SNP array	Genotyping	23
nssv15697162	copy number gain	199660	SNP array	Genotyping	15
nssv15698420	copy number gain	177296	SNP array	Genotyping	18
nssv15702008	copy number gain	200018	SNP array	Genotyping	18

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15613498	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15618212	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15622008	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15623562	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15623583	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15626063	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15627724	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15628979	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15631725	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15634324	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15634460	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15635257	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15636198	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15636608	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15637134	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15637999	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15640175	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15641672	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15642083	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15642102	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15642820	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15649624	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15652458	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15653110	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15653757	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15653874	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15658061	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15659547	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15664652	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15664693	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15665859	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15669639	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15669887	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15670148	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15670736	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15674537	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15677496	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15680408	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15680506	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15680558	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15681177	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15681384	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15681701	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15684321	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15688560	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15690616	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15694631	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15697162	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15698420	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15702008	Remapped	Perfect	NC_000003.12:g.(?_ 173522063)_(173582 390_?)dup	GRCh38.p12	First Pass	NC_000003.12	Chr3	173,522,063	173,582,390
nssv15613498	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15618212	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15622008	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15623562	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15623583	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15626063	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15627724	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15628979	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15631725	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15634324	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15634460	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15635257	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15636198	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15636608	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15637134	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15637999	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15640175	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15641672	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15642083	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15642102	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15642820	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15649624	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15652458	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15653110	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15653757	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15653874	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15658061	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15659547	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15664652	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15664693	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15665859	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15669639	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15669887	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15670148	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15670736	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15674537	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15677496	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15680408	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15680506	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15680558	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15681177	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15681384	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15681701	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15684321	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15688560	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15690616	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15694631	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15697162	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15698420	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180
nssv15702008	Submitted genomic		NC_000003.11:g.(?_ 173239853)_(173300 180_?)dup	GRCh37 (hg19)		NC_000003.11	Chr3	173,239,853	173,300,180

dbVar

Database of genomic structural variation

nsv4376485

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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