A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18044656



Internal ID20611696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:68773751..68774160hg38UCSC Ensembl
chr18:66440988..66441397hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516016
Supporting Variants
Samples
Known GenesCCDC102B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18044656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00185


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