A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701003



Internal ID124669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60100000..60118937hg38UCSC Ensembl
chr15:60392199..60411136hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818938
hg1918938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5517768
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701003
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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