A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585837



Internal ID347416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60897191..60897769hg38UCSC Ensembl
Outerchr16:60897004..60900864hg38UCSC Ensembl
Innerchr16:60931095..60931673hg19UCSC Ensembl
Outerchr16:60930908..60934768hg19UCSC Ensembl
Innerchr16:59488596..59489174hg18UCSC Ensembl
Outerchr16:59488409..59492269hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383861
hg193861
hg183861
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275094
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)essv2585837
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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