A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980572



Internal ID12635965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112647165..112819165hg38UCSC Ensembl
Innerchr9:115409445..115581445hg19UCSC Ensembl
Innerchr9:114449266..114621266hg18UCSC Ensembl
Innerchr9:112489000..112661000hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38172001
hg19172001
hg18172001
hg17172001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34739
Supporting Variants
SamplesNA19210
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980572
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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