A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980525



Internal ID12635879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112651324..112811301hg38UCSC Ensembl
Innerchr9:115413604..115573581hg19UCSC Ensembl
Innerchr9:114453425..114613402hg18UCSC Ensembl
Innerchr9:112493159..112653136hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38159978
hg19159978
hg18159978
hg17159978
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35051
Supporting Variants
SamplesNA19204
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980525
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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