A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585887



Internal ID347466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:91610173..91610742hg38UCSC Ensembl
Outerchr9:91609424..91611524hg38UCSC Ensembl
Innerchr9:94372455..94373024hg19UCSC Ensembl
Outerchr9:94371706..94373806hg19UCSC Ensembl
Innerchr9:93412276..93412845hg18UCSC Ensembl
Outerchr9:93411527..93413627hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382101
hg192101
hg182101
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275033
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)essv2585887
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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