A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100058



Internal ID20667098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33644206..33644601hg38UCSC Ensembl
chr3:33685698..33686093hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359934
Supporting Variants
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100058
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00098


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