A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694111



Internal ID117777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98250699..98290575hg38UCSC Ensembl
chr13:98902953..98942829hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3839877
hg1939877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5500382
Supporting Variants
Samples
Known GenesFARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694111
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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