A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555274



Internal ID15995997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67666398..67985501hg38UCSC Ensembl
Innerchr11:67433869..67752972hg19UCSC Ensembl
Innerchr11:67190445..67509548hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38319104
hg19319104
hg18319104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv778610
Samples
Known GenesALDH3B2, FAM86C2P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555274
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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