A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016202



Internal ID19105421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17630..82468hg38UCSC Ensembl
Innerchr5:17630..82583hg19UCSC Ensembl
Innerchr5:70630..135583hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3864839
hg1964954
hg1864954
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5513n100
Supporting Variantsnssv3633198
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)nsv1016202
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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