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

dbVar

Database of genomic structural variation

nsv6019976

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:89

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: 233 SVs from 51 studies. See in: genome view

Submitted genomic148,174,388-148,174,476

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6019976	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	148,174,388	148,174,476
nsv6019976	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	147,553,951	147,554,039

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17561897	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17561897	Submitted genomic		NC_000005.10:g.148 174388_148174476de l	GRCh38 (hg38)		NC_000005.10	Chr5	148,174,388	148,174,476
nssv17561897	Remapped	Perfect	NC_000005.9:g.1475 53951_147554039del	GRCh37.p13	First Pass	NC_000005.9	Chr5	147,553,951	147,554,039

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