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dbVar

Database of genomic structural variation

nsv5528906

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:224

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: 188 SVs from 32 studies. See in: genome view

Submitted genomic84,594,011-84,594,234

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5528906	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	84,594,011	84,594,234
nsv5528906	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	84,627,617	84,627,840

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17708335	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17708335	Submitted genomic		NC_000016.10:g.845 94011_84594234del	GRCh38 (hg38)		NC_000016.10	Chr16	84,594,011	84,594,234
nssv17708335	Remapped	Perfect	NC_000016.9:g.8462 7617_84627840del	GRCh37.p13	First Pass	NC_000016.9	Chr16	84,627,617	84,627,840

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)
nssv17708335	0.006	36	6404

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