A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097267



Internal ID20664307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17433096..17561276hg38UCSC Ensembl
chr3:17474588..17602768hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38128181
hg19128181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362111
Supporting Variants
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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