A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174819



Internal ID15873766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:69037338..69088127hg38UCSC Ensembl
Innerchr11:68804806..68855595hg19UCSC Ensembl
Innerchr11:68561382..68612171hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3850790
hg1950790
hg1850790
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555300
Supporting Variants
SamplesHGDP00336
Known GenesTPCN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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