A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692398



Internal ID116064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107791696..107796238hg38UCSC Ensembl
chr13:108444044..108448586hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg384543
hg194543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5509960
Supporting Variants
Samples
Known GenesFAM155A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692398
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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