A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933991



Internal ID22709310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70732919..70751414hg38UCSC Ensembl
chr13:71307051..71325546hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3818496
hg1918496
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379407
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933991
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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