A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408566



Internal ID187891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96328610..96328661hg38UCSC Ensembl
chr10:98088367..98088418hg19UCSC 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 Variantsnssv17038790
Samples
Known GenesDNTT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408566
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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