A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17378682



Internal ID22436552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26065437..26085281hg38UCSC Ensembl
chr13:26639575..26659419hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3819845
hg1919845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929282
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17378682
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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