A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585931



Internal ID347510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:137967399..137977165hg38UCSC Ensembl
Outerchr6:137964585..137977956hg38UCSC Ensembl
Innerchr6:138288536..138298302hg19UCSC Ensembl
Outerchr6:138285722..138299093hg19UCSC Ensembl
Innerchr6:138330229..138339995hg18UCSC Ensembl
Outerchr6:138327415..138340786hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg3813372
hg1913372
hg1813372
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275167
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)essv2585931
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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