A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3565497



Internal ID18863778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59679539..59744183hg38UCSC Ensembl
Innerchr18:57346771..57411415hg19UCSC Ensembl
Innerchr18:55497751..55562395hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3864645
hg1964645
hg1864645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059252
Supporting Variants
Samples
Known GenesCCBE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3565497
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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