A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406987



Internal ID186323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101808644..101808695hg38UCSC Ensembl
chr10:103568401..103568452hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037646
Samples
Known GenesMGEA5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406987
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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