A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033498



Internal ID19122719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:8554326..8702116hg38UCSC Ensembl
Innerchr5:8554438..8702228hg19UCSC Ensembl
Innerchr5:8607438..8755228hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38147791
hg19147791
hg18147791
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3639650, nssv3639651
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033498
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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