A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv577395



Internal ID16364804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:69050270..69208799hg38UCSC Ensembl
Innerchr18:66717507..66876036hg19UCSC Ensembl
Innerchr18:64868487..65027016hg18UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38158530
hg19158530
hg18158530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150277
Samples1780854441_A
Known GenesCCDC102B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv577395
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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