A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420619



Internal ID199716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:36899366..36899417hg38UCSC Ensembl
chr15:37191567..37191618hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701973
Samples
Known GenesMEIS2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420619
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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