A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476388



Internal ID254000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86970565..86970634hg38UCSC Ensembl
chr10:88730322..88730391hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17036781
Samples
Known GenesADIRF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476388
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