A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030034



Internal ID19119253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:681187..790474hg38UCSC Ensembl
Innerchr5:681302..790589hg19UCSC Ensembl
Innerchr5:734302..843589hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38109288
hg19109288
hg18109288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5523n100
Supporting Variantsnssv3745332
Samples
Known GenesTPPP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030034
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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