A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694724



Internal ID15431376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78915811..78927314hg38UCSC Ensembl
Innerchr18:76675811..76687314hg19UCSC Ensembl
Innerchr18:74776799..74788302hg18UCSC Ensembl
Innerchr18:74776799..74788302hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3811504
hg1911504
hg1811504
hg1711504
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521955
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694724
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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