A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785189



Internal ID16079145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134484754..134849175hg38UCSC Ensembl
Innerchr11:134354648..134719069hg19UCSC Ensembl
Innerchr11:133859858..134224279hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38364422
hg19364422
hg18364422
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556646
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785189
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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