A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577390



Internal ID16364799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69033015..69080331hg38UCSC Ensembl
Innerchr18:66700252..66747568hg19UCSC Ensembl
Innerchr18:64851232..64898548hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3847317
hg1947317
hg1847317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv886507
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577390
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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