nsv6304826 - dbVar Variant - NCBI

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nsv6304826

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:4,575

Description:nsv5502810 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: 102 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):33,734,067-33,738,641

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6304826	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	33,734,067	33,738,641
nsv6304826	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	33,755,613	33,760,187

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17674809	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17674809	Remapped	Perfect	NC_000011.10:g.337 34067_33738641del	GRCh38.p12	First Pass	NC_000011.10	Chr11	33,734,067	33,738,641
nssv17674809	Submitted genomic		NC_000011.9:g.3375 5613_33760187del	GRCh37 (hg19)		NC_000011.9	Chr11	33,755,613	33,760,187

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)
nssv17674809	0.012	74	6384

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