A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040483



Internal ID94696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123982837..123984754hg38UCSC Ensembl
chr10:125742353..125744270hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381918
hg191918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497470
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040483
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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