A curated catalogue of human genomic structural variation




Variant Details

Variant: esv274985



Internal ID1205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23632223..23632666hg38UCSC Ensembl
Outerchr14:23631250..23634912hg38UCSC Ensembl
Innerchr14:24101432..24101875hg19UCSC Ensembl
Outerchr14:24100459..24104121hg19UCSC Ensembl
Innerchr14:23171272..23171715hg18UCSC Ensembl
Outerchr14:23170299..23173961hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg383663
hg193663
hg183663
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585975
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)esv274985
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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