A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524947



Internal ID15105554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37494519..37494798hg38UCSC Ensembl
Innerchr18:35074482..35074761hg19UCSC Ensembl
Innerchr18:33328480..33328759hg18UCSC Ensembl
Innerchr18:33328480..33328759hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38280
hg19280
hg18280
hg17280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700965
Samples
Known GenesCELF4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524947
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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