A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492239



Internal ID269456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10091094..10124365hg38UCSC Ensembl
chr10:10133057..10166328hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3833272
hg1933272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492239
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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