A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039993



Internal ID94382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103196949..103205999hg38UCSC Ensembl
chr10:104956706..104965756hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg389051
hg199051
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563773
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039993
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001873


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