A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520543



Internal ID15447836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:38105289..38107932hg38UCSC Ensembl
Innerchr18:35685253..35687896hg19UCSC Ensembl
Innerchr18:33939251..33941894hg18UCSC Ensembl
Innerchr18:33939251..33941894hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382644
hg192644
hg182644
hg172644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697477
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520543
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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