A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565399



Internal ID18863680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:47842216..47868015hg38UCSC Ensembl
Innerchr18:45368587..45394386hg19UCSC Ensembl
Innerchr18:43622585..43648384hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3825800
hg1925800
hg1825800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066394
Supporting Variants
Samples
Known GenesSMAD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3565399
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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