A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275431



Internal ID348337
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585342, essv2585539
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)esv275431
Frequency
Sample Size1250
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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