A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5936048



Internal ID22711397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26762581..26768395hg38UCSC Ensembl
chr13:27336718..27342532hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg385815
hg195815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17381794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5936048
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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