A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556632



Internal ID16344041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479021..134865961hg38UCSC Ensembl
Innerchr11:134348915..134735855hg19UCSC Ensembl
Innerchr11:133854125..134241065hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38386941
hg19386941
hg18386941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv785176
Samples
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556632
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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