A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556616



Internal ID16344025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134474835..134851577hg38UCSC Ensembl
Innerchr11:134344729..134721471hg19UCSC Ensembl
Innerchr11:133849939..134226681hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38376743
hg19376743
hg18376743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv1176215
Samples1782681210_A
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556616
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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