A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039889



Internal ID94313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102087133..102092452hg38UCSC Ensembl
chr10:103846890..103852209hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg385320
hg195320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5477048
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039889
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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