A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174923



Internal ID15872634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98940429..98965361hg38UCSC Ensembl
Innerchr11:98811159..98836091hg19UCSC Ensembl
Innerchr11:98316369..98341301hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3824933
hg1924933
hg1824933
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556045
Supporting Variants
SamplesHGDP00003
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174923
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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