A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585720



Internal ID347299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:71614097..71614576hg38UCSC Ensembl
Outerchr3:71607777..71616207hg38UCSC Ensembl
Innerchr3:71663248..71663727hg19UCSC Ensembl
Outerchr3:71656928..71665358hg19UCSC Ensembl
Innerchr3:71745938..71746417hg18UCSC Ensembl
Outerchr3:71739618..71748048hg18UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg388431
hg198431
hg188431
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275502
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)essv2585720
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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