A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920219



Internal ID22695442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119862286..119862510hg38UCSC Ensembl
chr10:121621798..121622022hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369399
Samples
Known GenesMCMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920219
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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