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dbVar

Database of genomic structural variation

nsv5520877

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:97

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: 72 SVs from 22 studies. See in: genome view

Submitted genomic60,331,431-60,331,527

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5520877	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	60,331,431	60,331,527
nsv5520877	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	58,906,489	58,906,585

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17733423	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17733423	Submitted genomic		NC_000020.11:g.603 31431_60331527dup	GRCh38 (hg38)		NC_000020.11	Chr20	60,331,431	60,331,527
nssv17733423	Remapped	Perfect	NC_000020.10:g.589 06489_58906585dup	GRCh37.p13	First Pass	NC_000020.10	Chr20	58,906,489	58,906,585

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)
nssv17733423	0.076	487	6404

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