A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5422942



Internal ID201970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:47933776..47961000hg38UCSC Ensembl
chr10:47098903..47126094hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3827225
hg1927192
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17035034
Samples
Known GenesLINC00842
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5422942
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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