A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556469



Internal ID15997192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119308968..119314637hg38UCSC Ensembl
Innerchr11:119179678..119185347hg19UCSC Ensembl
Innerchr11:118684888..118690557hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg385670
hg195670
hg185670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784614
Samples
Known GenesMCAM, MIR6756
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556469
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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