A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015593



Internal ID19104810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:121600538..121706542hg38UCSC Ensembl
Innerchr5:120936233..121042237hg19UCSC Ensembl
Innerchr5:120964132..121070136hg18UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38106005
hg19106005
hg18106005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5806n100
Supporting Variantsnssv3648087
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)nsv1015593
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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