A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015814



Internal ID19105032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:685389..825526hg38UCSC Ensembl
Innerchr5:685504..825641hg19UCSC Ensembl
Innerchr5:738504..878641hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38140138
hg19140138
hg18140138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5524n100
Supporting Variantsnssv3633305, nssv3633309, nssv3745337, nssv3633307, nssv3633308, nssv3633306, nssv3633300, nssv3633304, nssv3633303, nssv3633302, nssv3633311, nssv3633310, nssv3633312, nssv3633301, nssv3745336
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)nsv1015814
Frequency
Sample Size11257
Observed Gain15
Observed Loss0
Observed Complex0
Frequencyn/a


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