A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152941



Internal ID15876292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:115132078..115408584hg38UCSC Ensembl
Innerchr4:116053234..116329740hg19UCSC Ensembl
Innerchr4:116272683..116549189hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38276507
hg19276507
hg18276507
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595255
Supporting Variants
SamplesHGDP00815
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152941
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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