A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778618



Internal ID16072574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68376815..68463772hg38UCSC Ensembl
Innerchr11:68144283..68231240hg19UCSC Ensembl
Innerchr11:67900859..67987816hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3886958
hg1986958
hg1886958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555285
Supporting Variants
Samples
Known GenesLRP5, PPP6R3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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