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dbVar

Database of genomic structural variation

nsv4673715

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:1,854

Description:nsv4623334 from DECIPHER Consensus CNVs. 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: 114 SVs from 31 studies. See in: genome view

Remapped(Score: Perfect):46,835,408-46,837,261

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4673715	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	46,835,408	46,837,261
nsv4673715	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	47,338,665	47,340,518

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16197516	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv16197516	Remapped	Perfect	NC_000019.10:g.(?_ 46835408)_(4683726 1_?)del	GRCh38.p12	First Pass	NC_000019.10	Chr19	46,835,408	46,837,261
nssv16197516	Submitted genomic		NC_000019.9:g.(?_4 7338665)_(47340518 _?)del	GRCh37 (hg19)		NC_000019.9	Chr19	47,338,665	47,340,518

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)
nssv16197516	0.025	48	1892

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