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

dbVar

Database of genomic structural variation

nsv5991951

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:62

Publication(s):Wu et al. 2021

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: 128 SVs from 27 studies. See in: genome view

Submitted genomic165,196,896-165,196,957

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5991951	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	165,196,896	165,196,957
nsv5991951	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	164,914,684	164,914,745

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17542967	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17542967	Submitted genomic		NC_000003.12:g.165 196896_165196957de l	GRCh38 (hg38)		NC_000003.12	Chr3	165,196,896	165,196,957
nssv17542967	Remapped	Perfect	NC_000003.11:g.164 914684_164914745de l	GRCh37.p13	First Pass	NC_000003.11	Chr3	164,914,684	164,914,745

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