A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5833747



Internal ID22608682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:81481088..81484724hg38UCSC Ensembl
chr2:81708212..81711848hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg383637
hg193637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488131
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5833747
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