A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686909



Internal ID110575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36737820..36783360hg38UCSC Ensembl
chr13:37311957..37357497hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3845541
hg1945541
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5510021
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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