A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039962



Internal ID94363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102828010..102828753hg38UCSC Ensembl
chr10:104587767..104588510hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38744
hg19744
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5507325
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039962
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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