A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556622



Internal ID16344031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134478080..134848323hg38UCSC Ensembl
Innerchr11:134347974..134718217hg19UCSC Ensembl
Innerchr11:133853184..134223427hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38370244
hg19370244
hg18370244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv785162
Samples
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556622
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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