A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1034606



Internal ID15887792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:66665377..66768198hg38UCSC Ensembl
Innerchr5:65961205..66064026hg19UCSC Ensembl
Innerchr5:65996961..66099782hg18UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38102822
hg19102822
hg18102822
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598406
Supporting Variants
Samples
Known GenesMAST4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1034606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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