A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020519



Internal ID19109738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121600538..121700376hg38UCSC Ensembl
Innerchr5:120936233..121036071hg19UCSC Ensembl
Innerchr5:120964132..121063970hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3899839
hg1999839
hg1899839
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5806n100
Supporting Variantsnssv3648086
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)nsv1020519
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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