A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018259



Internal ID19107476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:12790745..12935051hg38UCSC Ensembl
Innerchr5:12790857..12935163hg19UCSC Ensembl
Innerchr5:12843857..12988163hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38144307
hg19144307
hg18144307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638251
Samples
Known GenesCT49
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018259
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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