A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063322



Internal ID19152541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78128482..78170831hg38UCSC Ensembl
Innerchr18:75888482..75930831hg19UCSC Ensembl
Innerchr18:73989470..74031819hg18UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3842350
hg1942350
hg1842350
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3408n100
Supporting Variantsnssv3563046
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)nsv1063322
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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