A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565349



Internal ID18863630
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 StatusS
Merged Variantsnsv1063205
Supporting Variants
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)nssv3565349
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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