A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060346



Internal ID19149565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:42098492..42162738hg38UCSC Ensembl
Innerchr18:39678456..39742702hg19UCSC Ensembl
Innerchr18:37932454..37996700hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3864247
hg1964247
hg1864247
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3343n100
Supporting Variantsnssv3565350
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)nsv1060346
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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