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dbVar

Database of genomic structural variation

nsv6121805

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:1,280

Description:nsv5480729 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: 253 SVs from 45 studies. See in: genome view

Remapped(Score: Perfect):154,662,787-154,664,066

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6121805	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	154,662,787	154,664,066
nsv6121805	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	154,454,497	154,455,776

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17654088	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17654088	Remapped	Perfect	NC_000007.14:g.154 662787_154664066de l	GRCh38.p12	First Pass	NC_000007.14	Chr7	154,662,787	154,664,066
nssv17654088	Submitted genomic		NC_000007.13:g.154 454497_154455776de l	GRCh37 (hg19)		NC_000007.13	Chr7	154,454,497	154,455,776

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)
nssv17654088	0.882	5647	6404

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