A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485970



Internal ID263349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92553188..92561291hg38UCSC Ensembl
chr10:94312945..94321048hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg388104
hg198104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037904
Samples
Known GenesIDE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485970
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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