A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043662



Internal ID20610702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69821963..69822333hg38UCSC Ensembl
chr18:67489199..67489569hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524211
Supporting Variants
Samples
Known GenesDOK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00089


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