A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5400059



Internal ID179443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96260509..96260560hg38UCSC Ensembl
chr10:98020266..98020317hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038788
Samples
Known GenesBLNK
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5400059
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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