A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063351



Internal ID19152570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59539397..59562655hg38UCSC Ensembl
Innerchr18:57206629..57229887hg19UCSC Ensembl
Innerchr18:55357609..55380867hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3823259
hg1923259
hg1823259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3365n100
Supporting Variantsnssv3565493
Samples
Known GenesCCBE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063351
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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