A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744709



Internal ID16038665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:22318503..22326834hg38UCSC Ensembl
Innerchr10:22607432..22615763hg19UCSC Ensembl
Innerchr10:22647438..22655769hg18UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg388332
hg198332
hg188332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550208
Supporting Variants
Samples
Known GenesBMI1, COMMD3, COMMD3-BMI1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744709
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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