A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17694471



Internal ID118137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:94773781..94774389hg38UCSC Ensembl
chr13:95426035..95426643hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5512102
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17694471
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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