A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698789



Internal ID15088755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:64371134..64382934hg38UCSC Ensembl
Innerchr8:65283691..65295491hg19UCSC Ensembl
Innerchr8:65446245..65458045hg18UCSC Ensembl
Innerchr8:65446245..65458045hg17UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3811801
hg1911801
hg1811801
hg1711801
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523097
Supporting Variants
Samples
Known GenesLINC00966, MIR124-2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698789
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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