A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019396



Internal ID19108614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17549857..17700971hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg18151115
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5582n100
Supporting Variantsnssv3638410
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019396
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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