A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176223



Internal ID15853876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479860..134864402hg38UCSC Ensembl
Innerchr11:134349754..134734296hg19UCSC Ensembl
Innerchr11:133854964..134239506hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38384543
hg19384543
hg18384543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556637
Supporting Variants
Samples1780854467_A
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176223
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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