A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476653



Internal ID254258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78882717..78882782hg38UCSC Ensembl
chr10:80642474..80642539hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476653
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer