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

dbVar

Database of genomic structural variation

nsv4448018

Organism: Homo sapiens

Study:nstd175 (Genome in a Bottle)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:307

Description:SVTYPE=DEL;REPTYPE=SIMPLEDEL
Publication(s):Genome in a Bottle

Links to Other Resources

Overlapping Genes

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: 160 SVs from 50 studies. See in: genome view

Remapped(Score: Perfect):23,899,565-23,899,871

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4448018	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	23,899,565	23,899,871
nsv4448018	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	23,910,886	23,911,192

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15767150	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15767150	Remapped	Perfect	NC_000016.10:g.238 99565_23899871del	GRCh38.p12	First Pass	NC_000016.10	Chr16	23,899,565	23,899,871
nssv15767150	Submitted genomic		NC_000016.9:g.2391 0886_23911192del	GRCh37 (hg19)		NC_000016.9	Chr16	23,910,886	23,911,192

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

You are here: NCBI