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dbVar

Database of genomic structural variation

nsv5469180

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:553

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

Submitted genomic39,007,679-39,008,231

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5469180	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	39,007,679	39,008,231
nsv5469180	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	39,007,781	39,008,333

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16964839	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16964839	Submitted genomic		NC_000005.10:g.390 07679_39008231del	GRCh38 (hg38)		NC_000005.10	Chr5	39,007,679	39,008,231
nssv16964839	Remapped	Perfect	NC_000005.9:g.3900 7781_39008333del	GRCh37.p13	First Pass	NC_000005.9	Chr5	39,007,781	39,008,333

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)
nssv16964839	<0.001	1	6404

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