A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397760



Internal ID177164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42918748..42918763hg38UCSC Ensembl
chr10:43414196..43414211hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397760
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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