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dbVar

Database of genomic structural variation

nsv6632306

Organism: Homo sapiens

Study:nstd224 (Zarrei et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:3
Validation:Not tested
Clinical Assertions: No
Region Size:21,351

Publication(s):Zarrei et al. 2023

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: 301 SVs from 44 studies. See in: genome view

Remapped(Score: Perfect):114,308,962-114,330,312

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6632306	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	114,308,962	114,330,312
nsv6632306	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	115,321,191	115,342,541

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18291798	deletion	OSC3834	SNP array	Probe signal intensity	8
nssv18293863	deletion	OSC4162	SNP array	Probe signal intensity	6
nssv18325378	deletion	OSC1758	SNP array	Probe signal intensity	10

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18291798	Remapped	Perfect	NC_000008.11:g.(?_ 114308962)_(114330 312_?)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	114,308,962	114,330,312
nssv18293863	Remapped	Perfect	NC_000008.11:g.(?_ 114308962)_(114330 312_?)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	114,308,962	114,330,312
nssv18325378	Remapped	Perfect	NC_000008.11:g.(?_ 114308962)_(114330 312_?)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	114,308,962	114,330,312
nssv18291798	Submitted genomic		NC_000008.10:g.(?_ 115321191)_(115342 541_?)del	GRCh37 (hg19)		NC_000008.10	Chr8	115,321,191	115,342,541
nssv18293863	Submitted genomic		NC_000008.10:g.(?_ 115321191)_(115342 541_?)del	GRCh37 (hg19)		NC_000008.10	Chr8	115,321,191	115,342,541
nssv18325378	Submitted genomic		NC_000008.10:g.(?_ 115321191)_(115342 541_?)del	GRCh37 (hg19)		NC_000008.10	Chr8	115,321,191	115,342,541

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

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