A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686632



Internal ID110298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31054889..31055113hg38UCSC Ensembl
chr13:31629026..31629250hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511748
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686632
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.014063


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