A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585721



Internal ID347300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:132677128..132680140hg38UCSC Ensembl
Outerchr6:132675537..132680326hg38UCSC Ensembl
Innerchr6:132998267..133001279hg19UCSC Ensembl
Outerchr6:132996676..133001465hg19UCSC Ensembl
Innerchr6:133039960..133042972hg18UCSC Ensembl
Outerchr6:133038369..133043158hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg384790
hg194790
hg184790
Variant TypeCNV loss
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275102
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)essv2585721
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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