A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016567



Internal ID19105786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134049828..134081206hg38UCSC Ensembl
Innerchr8:135062071..135093449hg19UCSC Ensembl
Innerchr8:135131253..135162631hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3831379
hg1931379
hg1831379
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7324n100
Supporting Variantsnssv3692715, nssv3692713, nssv3692710, nssv3692714, nssv3692711, nssv3692712
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)nsv1016567
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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