A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043661



Internal ID20610701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:69821592..69828122hg38UCSC Ensembl
chr18:67488828..67495358hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg386531
hg196531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6531664
Supporting Variants
Samples
Known GenesDOK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043661
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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