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dbVar

Database of genomic structural variation

nsv4650483

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:30,913

Description:nsv4261520 from gnomAD Structural Variants. 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: 1070 SVs from 81 studies. See in: genome view

Remapped(Score: Perfect):40,833,387-40,864,299

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4650483	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000019.10	Chr19	40,833,387	40,864,299
nsv4650483	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000019.9	Chr19	41,339,292	41,370,204

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16177732	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16177732	Remapped	Perfect	NC_000019.10:g.408 33387_40864299del	GRCh38.p12	First Pass	NC_000019.10	Chr19	40,833,387	40,864,299
nssv16177732	Submitted genomic		NC_000019.9:g.4133 9292_41370204del	GRCh37 (hg19)		NC_000019.9	Chr19	41,339,292	41,370,204

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)
nssv16177732	0.036	787	21674

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