A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850692



Internal ID22625627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63497565..63519078hg38UCSC Ensembl
chr10:65257325..65278838hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3821514
hg1921514
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459832
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850692
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