A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585342



Internal ID346921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28835239..28837240hg38UCSC Ensembl
Outerchr10:28835091..28841777hg38UCSC Ensembl
Innerchr10:29124168..29126169hg19UCSC Ensembl
Outerchr10:29124020..29130706hg19UCSC Ensembl
Innerchr10:29164174..29166175hg18UCSC Ensembl
Outerchr10:29164026..29170712hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg386687
hg196687
hg186687
Variant TypeCNV gain
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275431
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)essv2585342
Frequency
Sample Size1250
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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