A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174958



Internal ID15534334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119106009..119188695hg38UCSC Ensembl
Innerchr11:118976719..119059404hg19UCSC Ensembl
Innerchr11:118481929..118564614hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3882687
hg1982686
hg1882686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556466
Supporting Variants
SamplesNINDS_60
Known GenesABCG4, C2CD2L, HINFP, NLRX1, PDZD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174958
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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