A curated catalogue of human genomic structural variation




Variant Details

Variant: essv2585123



Internal ID16
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 OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv275537
Supporting Variants
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)essv2585123
Frequency
Sample Size1250
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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