A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519742



Internal ID15100349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:58714893..58749461hg38UCSC Ensembl
Innerchr18:56382125..56416693hg19UCSC Ensembl
Innerchr18:54533105..54567673hg18UCSC Ensembl
Innerchr18:54533105..54567673hg17UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3834569
hg1934569
hg1834569
hg1734569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678987, nssv658091
Samples
Known GenesMALT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519742
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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