A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701045



Internal ID124711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73822998..73847618hg38UCSC Ensembl
chr15:74115339..74139959hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3824621
hg1924621
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5521251
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701045
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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