A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023689



Internal ID19112906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:659283..825526hg38UCSC Ensembl
Innerchr5:659398..825641hg19UCSC Ensembl
Innerchr5:712398..878641hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38166244
hg19166244
hg18166244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5524n100
Supporting Variantsnssv3633239, nssv3633238
Samples
Known GenesTPPP, ZDHHC11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023689
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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