A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483332



Internal ID260771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72902155..72902288hg38UCSC Ensembl
chr10:74661913..74662046hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035989
Samples
Known GenesOIT3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483332
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