A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021350



Internal ID19110567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:668727..825526hg38UCSC Ensembl
Innerchr5:668842..825641hg19UCSC Ensembl
Innerchr5:721842..878641hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38156800
hg19156800
hg18156800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5524n100
Supporting Variantsnssv3633250, nssv3633249
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)nsv1021350
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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