A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17040466



Internal ID94685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123722801..123723028hg38UCSC Ensembl
chr10:125482317..125482544hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38228
hg19228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503976
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17040466
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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