A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032824



Internal ID18775358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:335214..449516hg38UCSC Ensembl
Innerchr5:335329..449631hg19UCSC Ensembl
Innerchr5:388329..502631hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38114303
hg19114303
hg18114303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633216
Samples
Known GenesAHRR, C5orf55, EXOC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032824
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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