A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565396



Internal ID18863677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:47833641..47878121hg38UCSC Ensembl
Innerchr18:45360012..45404492hg19UCSC Ensembl
Innerchr18:43614010..43658490hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3844481
hg1944481
hg1844481
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058673
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)nssv3565396
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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