A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5491120



Internal ID268364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57749116..57781323hg38UCSC Ensembl
chr10:59508876..59541083hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3832208
hg1932208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032933
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5491120
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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