A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024461



Internal ID19113678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:670630..787933hg38UCSC Ensembl
Innerchr5:670745..788048hg19UCSC Ensembl
Innerchr5:723745..841048hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38117304
hg19117304
hg18117304
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5523n100
Supporting Variantsnssv3633256, nssv3633255
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)nsv1024461
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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