A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17692685



Internal ID116351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:104697694..104912939hg38UCSC Ensembl
chr13:105350045..105565290hg19UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg38215246
hg19215246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497359
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17692685
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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