A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691122



Internal ID114788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:89349884..89366260hg38UCSC Ensembl
chr13:90002138..90018514hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3816377
hg1916377
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691122
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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