A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705462



Internal ID15095428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22120559..22131002hg38UCSC Ensembl
Innerchr8:21978072..21988515hg19UCSC Ensembl
Innerchr8:22034017..22044460hg18UCSC Ensembl
Innerchr8:22034017..22044460hg17UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3810444
hg1910444
hg1810444
hg1710444
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519698
Supporting Variants
Samples
Known GenesHR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705462
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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