A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17700886



Internal ID124552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58226903..58292667hg38UCSC Ensembl
chr15:58519102..58584866hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3865765
hg1965765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17700886
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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