A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944105



Internal ID22719564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110930166..111008240hg38UCSC Ensembl
chr13:111582513..111660587hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3878075
hg1978075
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365050
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944105
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