A curated catalogue of human genomic structural variation




Variant Details

Variant: esv275537



Internal ID1757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76059272..76059442hg38UCSC Ensembl
Outerchr10:76058277..76059598hg38UCSC Ensembl
Innerchr10:77819030..77819200hg19UCSC Ensembl
Outerchr10:77818035..77819356hg19UCSC Ensembl
Innerchr10:77489036..77489206hg18UCSC Ensembl
Outerchr10:77488041..77489362hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381322
hg191322
hg181322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv2585123
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIdentification of germline Changes in Copy Number (IgC2N)
PlatformAffymetrix SNP 6.0
Comments
ReferenceBanerjee_et_al_2011
Pubmed ID21479260
Accession Number(s)esv275537
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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