A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659622



Internal ID15049588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76507072..76927895hg38UCSC Ensembl
Innerchr7:76136389..76557212hg19UCSC Ensembl
Innerchr7:75974325..76395148hg18UCSC Ensembl
Innerchr7:75781040..76201863hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38420824
hg19420824
hg18420824
hg17420824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517634
Supporting Variants
Samples
Known GenesLOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659622
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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