A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858415



Internal ID22633350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19838807..19840106hg38UCSC Ensembl
chr13:20412947..20414246hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465763
Samples
Known GenesZMYM5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858415
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