A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513190



Internal ID289721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119652340..119655494hg38UCSC Ensembl
chr10:121411852..121415006hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383155
hg193155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17039337
Samples
Known GenesBAG3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513190
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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