A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063205



Internal ID19152424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42098492..42161097hg38UCSC Ensembl
Innerchr18:39678456..39741061hg19UCSC Ensembl
Innerchr18:37932454..37995059hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3862606
hg1962606
hg1862606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3343n100
Supporting Variantsnssv3565349
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)nsv1063205
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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