A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566455



Internal ID18518050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68019389..68852518hg38UCSC Ensembl
Innerchr18:65686626..66519755hg19UCSC Ensembl
Innerchr18:63837606..64670735hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38833130
hg19833130
hg18833130
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056926
Supporting Variants
Samples
Known GenesCCDC102B, TMX3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566455
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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