A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980573



Internal ID12635964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112651165..112811165hg38UCSC Ensembl
Innerchr9:115413445..115573445hg19UCSC Ensembl
Innerchr9:114453266..114613266hg18UCSC Ensembl
Innerchr9:112493000..112653000hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38160001
hg19160001
hg18160001
hg17160001
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 Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980573
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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