A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5485695



Internal ID263079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49405648..49411603hg38UCSC Ensembl
chr10:50613694..50619649hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg385956
hg195956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036058
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5485695
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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