A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678987



Internal ID15068953
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519742
Supporting Variants
Samples
Known GenesMALT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678987
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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