A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556610



Internal ID15997333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134381883..134555421hg38UCSC Ensembl
Innerchr11:134251777..134425315hg19UCSC Ensembl
Innerchr11:133756987..133930525hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38173539
hg19173539
hg18173539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2206n54
Supporting Variantsnssv785150
Samples
Known GenesB3GAT1, LOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556610
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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