A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405620



Internal ID184963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123372082..123372126hg38UCSC Ensembl
chr10:125131598..125131642hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405620
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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