A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585811



Internal ID347390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69889330..69895773hg38UCSC Ensembl
Outerchr17:69889125..69895865hg38UCSC Ensembl
Innerchr17:67885471..67891914hg19UCSC Ensembl
Outerchr17:67885266..67892006hg19UCSC Ensembl
Innerchr17:65397066..65403509hg18UCSC Ensembl
Outerchr17:65396861..65403601hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg386741
hg196741
hg186741
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275207
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)essv2585811
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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