A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016102



Internal ID19105320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12525636..12669423hg38UCSC Ensembl
Innerchr5:12525748..12669535hg19UCSC Ensembl
Innerchr5:12578748..12722535hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38143788
hg19143788
hg18143788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5571n100
Supporting Variantsnssv3638210
Samples
Known GenesCT49
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016102
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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