A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836790



Internal ID22611725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72524098..72525431hg38UCSC Ensembl
chr3:72573249..72574582hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381334
hg191334
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17494750, nssv17494751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836790
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