A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699997



Internal ID15089963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101006159..101075321hg38UCSC Ensembl
Innerchr8:102018387..102087549hg19UCSC Ensembl
Innerchr8:102087563..102156725hg18UCSC Ensembl
Innerchr8:102087563..102156725hg17UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3869163
hg1969163
hg1869163
hg1769163
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524119
Supporting Variants
Samples
Known GenesFLJ42969
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699997
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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