A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17688209



Internal ID111875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:59132019..59132373hg38UCSC Ensembl
chr13:59706153..59706507hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17688209
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00359


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