A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5838913



Internal ID22613848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24501465..24502655hg38UCSC Ensembl
chr4:24503088..24504278hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17493372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5838913
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