A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17686995



Internal ID110661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:38410363..38410547hg38UCSC Ensembl
chr13:38984500..38984684hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508861
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17686995
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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