A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585932



Internal ID347511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111964426..111964482hg38UCSC Ensembl
Outerchr9:111959966..111965040hg38UCSC Ensembl
Innerchr9:114726706..114726762hg19UCSC Ensembl
Outerchr9:114722246..114727320hg19UCSC Ensembl
Innerchr9:113766527..113766583hg18UCSC Ensembl
Outerchr9:113762067..113767141hg18UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385075
hg195075
hg185075
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275402
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)essv2585932
Frequency
Sample Size1250
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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