A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17614196



Internal ID21806243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112164040..112164268hg38UCSC Ensembl
chr13:112818354..112818582hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17614196
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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