A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038334



Internal ID93284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86534158..86536998hg38UCSC Ensembl
chr10:88293915..88296755hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382841
hg192841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5480223
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038334
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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