A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763439



Internal ID15710709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:412505..431554hg38UCSC Ensembl
Innerchr11:412505..431554hg19UCSC Ensembl
Innerchr11:402505..421554hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3819050
hg1919050
hg1819050
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552825
Supporting Variants
Samples
Known GenesANO9, SIGIRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763439
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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