A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362111



Internal ID21019664
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 StatusM
Merged Variants
Supporting Variantsnssv18097267
Samples
Known GenesTBC1D5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362111
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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