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dbVar

Database of genomic structural variation

nsv6631128

Organism: Homo sapiens

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

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:243,548

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: 1893 SVs from 96 studies. See in: genome view

Remapped(Score: Perfect):167,953,372-168,196,919

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6631128	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	167,953,372	168,196,919
nsv6631128	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	168,354,052	168,597,599

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv18317435	duplication	OSC8467	SNP array	Probe signal intensity	9
nssv18319178	duplication	OSC8768	SNP array	Probe signal intensity	7

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv18317435	Remapped	Perfect	NC_000006.12:g.(?_ 167953372)_(168196 919_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	167,953,372	168,196,919
nssv18319178	Remapped	Perfect	NC_000006.12:g.(?_ 167953372)_(168196 919_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	167,953,372	168,196,919
nssv18317435	Submitted genomic		NC_000006.11:g.(?_ 168354052)_(168597 599_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	168,354,052	168,597,599
nssv18319178	Submitted genomic		NC_000006.11:g.(?_ 168354052)_(168597 599_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	168,354,052	168,597,599

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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