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dbVar

Database of genomic structural variation

nsv6301677

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:331

Description:nsv6141223 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: 155 SVs from 52 studies. See in: genome view

Remapped(Score: Perfect):105,119,967-105,120,297

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6301677	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	105,119,967	105,120,297
nsv6301677	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	105,567,842	105,568,172

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17669813	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17669813	Remapped	Perfect	NC_000006.12:g.105 119967_105120297de l	GRCh38.p12	First Pass	NC_000006.12	Chr6	105,119,967	105,120,297
nssv17669813	Submitted genomic		NC_000006.11:g.105 567842_105568172de l	GRCh37 (hg19)		NC_000006.11	Chr6	105,567,842	105,568,172

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)
nssv17669813	0.013	83	6404

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