A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17687366



Internal ID111032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:44833665..44853084hg38UCSC Ensembl
chr13:45407801..45427220hg19UCSC Ensembl
Cytoband13q14.12
Allele length
AssemblyAllele length
hg3819420
hg1919420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5502025
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17687366
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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