A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016359



Internal ID19105578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25116916..25141819hg38UCSC Ensembl
Innerchr8:24974431..24999334hg19UCSC Ensembl
Innerchr8:25030348..25055251hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3824904
hg1924904
hg1824904
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7144n100
Supporting Variantsnssv3685442
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)nsv1016359
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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