A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv886508



Internal ID16180464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69033015..69084931hg38UCSC Ensembl
Innerchr18:66700252..66752168hg19UCSC Ensembl
Innerchr18:64851232..64903148hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3851917
hg1951917
hg1851917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv577391
Supporting Variants
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv886508
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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