A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524760



Internal ID15105367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:58749461..58755636hg38UCSC Ensembl
Innerchr18:56416693..56422868hg19UCSC Ensembl
Innerchr18:54567673..54573848hg18UCSC Ensembl
Innerchr18:54567673..54573848hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg386176
hg196176
hg186176
hg176176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700751
Samples
Known GenesMALT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524760
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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