A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17598053



Internal ID21790097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113600655..113600747hg38UCSC Ensembl
chr13:114254970..114255062hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025739
Supporting Variants
Samples
Known GenesTFDP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17598053
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