A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692390



Internal ID116056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107655093..107660418hg38UCSC Ensembl
chr13:108307441..108312766hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385326
hg195326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511654
Supporting Variants
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692390
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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