A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944655



Internal ID22720123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:67964834..67980235hg38UCSC Ensembl
chr13:68538966..68554367hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3815402
hg1915402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379880
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944655
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