A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18100060



Internal ID20667100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:33652728..33653146hg38UCSC Ensembl
chr3:33694220..33694638hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38419
hg19419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362005
Supporting Variants
Samples
Known GenesCLASP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18100060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00139


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