A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848920



Internal ID22623855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125980930..125982390hg38UCSC Ensembl
chr10:127669499..127670959hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg381461
hg191461
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467169, nssv17458988
Samples
Known GenesFANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848920
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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