A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691932



Internal ID115598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62741624..63058758hg38UCSC Ensembl
chr13:63315757..63632891hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38317135
hg19317135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511623
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691932
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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