A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275227



Internal ID348133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36015774..36016225hg38UCSC Ensembl
Outerchr14:36013282..36017872hg38UCSC Ensembl
Innerchr14:36484980..36485431hg19UCSC Ensembl
Outerchr14:36482488..36487078hg19UCSC Ensembl
Innerchr14:35554731..35555182hg18UCSC Ensembl
Outerchr14:35552239..35556829hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg384591
hg194591
hg184591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585446
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)esv275227
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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