A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763440



Internal ID15710710
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 loss
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)nssv763440
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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