A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585179



Internal ID346758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:67780147..67780780hg38UCSC Ensembl
Outerchr13:67777163..67783977hg38UCSC Ensembl
Innerchr13:68354279..68354912hg19UCSC Ensembl
Outerchr13:68351295..68358109hg19UCSC Ensembl
Innerchr13:67252280..67252913hg18UCSC Ensembl
Outerchr13:67249296..67256110hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg386815
hg196815
hg186815
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275499
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)essv2585179
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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