A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1026290



Internal ID16320246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:16980748..17012666hg38UCSC Ensembl
Innerchr5:16980857..17012775hg19UCSC Ensembl
Innerchr5:17033857..17065775hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3831919
hg1931919
hg1831919
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv597311
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1026290
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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