A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597796



Internal ID21789839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113144784..113144949hg38UCSC Ensembl
chr13:113799098..113799263hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024406
Supporting Variants
Samples
Known GenesF10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597796
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