A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585963



Internal ID347542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:39410336..39413391hg38UCSC Ensembl
Outerchr20:39405808..39417473hg38UCSC Ensembl
Innerchr20:38038979..38042034hg19UCSC Ensembl
Outerchr20:38034451..38046116hg19UCSC Ensembl
Innerchr20:37472393..37475448hg18UCSC Ensembl
Outerchr20:37467865..37479530hg18UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3811666
hg1911666
hg1811666
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275532
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)essv2585963
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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