A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174842



Internal ID15877684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81606904..81652893hg38UCSC Ensembl
Innerchr11:81317946..81363935hg19UCSC Ensembl
Innerchr11:80995594..81041583hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3845990
hg1945990
hg1845990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555484
Supporting Variants
SamplesHGDP01029
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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