A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019680



Internal ID19108898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:30291894..30431012hg38UCSC Ensembl
Innerchr5:30292001..30431119hg19UCSC Ensembl
Innerchr5:30327758..30466876hg18UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38139119
hg19139119
hg18139119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5617n100
Supporting Variantsnssv3745867
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)nsv1019680
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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