A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744010



Internal ID16037966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11964359..12034044hg38UCSC Ensembl
Innerchr10:12006358..12076043hg19UCSC Ensembl
Innerchr10:12046364..12116049hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3869686
hg1969686
hg1869686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549968
Supporting Variants
Samples
Known GenesUPF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744010
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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