Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv4654172

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:792

Description:nsv4100710 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: 111 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):146,105,471-146,106,262

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4654172	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	146,105,471	146,106,262
nsv4654172	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	147,026,623	147,027,414

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16156383	deletion	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16156383	Remapped	Perfect	NC_000004.12:g.146 105471_146106262de l	GRCh38.p12	First Pass	NC_000004.12	Chr4	146,105,471	146,106,262
nssv16156383	Submitted genomic		NC_000004.11:g.147 026623_147027414de l	GRCh37 (hg19)		NC_000004.11	Chr4	147,026,623	147,027,414

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)
nssv16156383	0.193	4154	21534

You are here: NCBI