A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483377



Internal ID260814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89540043..89550174hg38UCSC Ensembl
chr10:91299800..91309931hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3810132
hg1910132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483377
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