A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1153441



Internal ID15872964
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10873309..11268255hg38UCSC Ensembl
Innerchr4:10874933..11269879hg19UCSC Ensembl
Innerchr4:10484031..10878977hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38394947
hg19394947
hg18394947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593732
Supporting Variants
SamplesHGDP00088
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1153441
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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