A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275505



Internal ID348411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:58949476..58950423hg38UCSC Ensembl
Outerchr20:58943396..58950713hg38UCSC Ensembl
Innerchr20:57524531..57525478hg19UCSC Ensembl
Outerchr20:57518451..57525768hg19UCSC Ensembl
Innerchr20:56957926..56958873hg18UCSC Ensembl
Outerchr20:56951846..56959163hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg387318
hg197318
hg187318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585788
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)esv275505
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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