A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520275



Internal ID15447568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:68863126..68903186hg38UCSC Ensembl
Innerchr18:66530363..66570423hg19UCSC Ensembl
Innerchr18:64681343..64721403hg18UCSC Ensembl
Innerchr18:64681343..64721403hg17UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3840061
hg1940061
hg1840061
hg1740061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684755, nssv662321, nssv690070
Samples
Known GenesCCDC102B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520275
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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