A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5406324



Internal ID185664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62865752..62865803hg38UCSC Ensembl
chr10:64625512..64625563hg19UCSC Ensembl
Cytoband10q21.3
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 Variantsnssv17034012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5406324
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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