A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093973



Internal ID20661013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140077823..140078467hg38UCSC Ensembl
chr3:139796665..139797309hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38645
hg19645
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367427
Supporting Variants
Samples
Known GenesCLSTN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093973
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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