A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv884912



Internal ID16178868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:59539473..59557547hg38UCSC Ensembl
Innerchr18:57206705..57224779hg19UCSC Ensembl
Innerchr18:55357685..55375759hg18UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3818075
hg1918075
hg1818075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577053
Supporting Variants
Samples
Known GenesCCBE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv884912
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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