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dbVar

Database of genomic structural variation

nsv5531657

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:60

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: 105 SVs from 23 studies. See in: genome view

Submitted genomic27,692,825-27,692,884

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5531657	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	27,692,825	27,692,884
nsv5531657	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	27,704,146	27,704,205

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17706283	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17706283	Submitted genomic		NC_000016.10:g.276 92825_27692884del	GRCh38 (hg38)		NC_000016.10	Chr16	27,692,825	27,692,884
nssv17706283	Remapped	Perfect	NC_000016.9:g.2770 4146_27704205del	GRCh37.p13	First Pass	NC_000016.9	Chr16	27,704,146	27,704,205

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)
nssv17706283	<0.001	3	6402

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