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

dbVar

Database of genomic structural variation

nsv5528090

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:19,305

Publication(s):Byrska-Bishop et al. 2022

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: 594 SVs from 71 studies. See in: genome view

Submitted genomic165,396-184,700

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5528090	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	165,396	184,700
nsv5528090	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	215,395	234,699

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17705658	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17705658	Submitted genomic		NC_000016.10:g.165 396_184700del	GRCh38 (hg38)		NC_000016.10	Chr16	165,396	184,700
nssv17705658	Remapped	Perfect	NC_000016.9:g.2153 95_234699del	GRCh37.p13	First Pass	NC_000016.9	Chr16	215,395	234,699

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17705658	0.004	23	6400

You are here: NCBI