A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549968



Internal ID16337377
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 StatusM
Merged Variantsdgv955n54
Supporting Variantsnssv744010
Samples
Known GenesUPF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549968
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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