A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850891



Internal ID22625826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124874274..124875273hg38UCSC Ensembl
chr10:126562843..126563842hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17457384, nssv17459448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850891
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