A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372956



Internal ID22598625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34351218..34351271hg38UCSC Ensembl
chr13:34925355..34925408hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5938018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372956
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