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dbVar

Database of genomic structural variation

nsv6304781

Organism: Homo sapiens

Study:nstd186 (NCBI Curated Common Structural Variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:5,501

Description:nsv6141214 from Byrska-Bishop et. al 2021. For a full list of variants now included in nstd186, refer to the mapping file provided here.

Links to Other Resources

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: 115 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):26,666,500-26,672,000

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6304781	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	26,666,500	26,672,000
nsv6304781	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	26,666,728	26,672,228

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17667008	duplication	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17667008	Remapped	Perfect	NC_000006.12:g.266 66500_26672000dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	26,666,500	26,672,000
nssv17667008	Submitted genomic		NC_000006.11:g.266 66728_26672228dup	GRCh37 (hg19)		NC_000006.11	Chr6	26,666,728	26,672,228

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17667008	0.718	4340	6048

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