A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694943



Internal ID15084909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36309618..36322637hg38UCSC Ensembl
Innerchr18:33889581..33902600hg19UCSC Ensembl
Innerchr18:32143579..32156598hg18UCSC Ensembl
Innerchr18:32143579..32156598hg17UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3813020
hg1913020
hg1813020
hg1713020
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522170
Supporting Variants
Samples
Known GenesFHOD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694943
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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