A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174831



Internal ID15534622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:72570840..72625520hg38UCSC Ensembl
Innerchr11:72281884..72336564hg19UCSC Ensembl
Innerchr11:71959532..72014212hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3854681
hg1954681
hg1854681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555406
Supporting Variants
SamplesNINDS_98
Known GenesMIR139, PDE2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174831
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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