A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555558



Internal ID328712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86545775..86545826hg38UCSC Ensembl
chr10:88305532..88305583hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg381312
hg191312
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17038335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555558
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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