A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565426



Internal ID18863707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:47861352..47874989hg38UCSC Ensembl
Innerchr18:45387723..45401360hg19UCSC Ensembl
Innerchr18:43641721..43655358hg18UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg3813638
hg1913638
hg1813638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059902
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)nssv3565426
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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