A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700751



Internal ID15090717
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524760
Supporting Variants
Samples
Known GenesMALT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700751
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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