A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032584



Internal ID18775118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:375290..809679hg38UCSC Ensembl
Innerchr5:375405..809794hg19UCSC Ensembl
Innerchr5:428405..862794hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38434390
hg19434390
hg18434390
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633220
Samples
Known GenesAHRR, C5orf55, CEP72, EXOC3, LOC100996325, MIR4456, PP7080, SLC9A3, TPPP, ZDHHC11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032584
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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