A curated catalogue of human genomic structural variation




Variant Details

Variant: esv35051



Internal ID12644401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112621052..112811301hg38UCSC Ensembl
Innerchr9:115383332..115573581hg19UCSC Ensembl
Innerchr9:114423153..114613402hg18UCSC Ensembl
Innerchr9:112462887..112653136hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38190250
hg19190250
hg18190250
hg17190250
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv262e55
Supporting Variantsessv6986011, essv6980525, essv6980524
SamplesNA19204
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv35051
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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