A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691220



Internal ID114886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:100615568..100616368hg38UCSC Ensembl
chr13:101267822..101268622hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5503923
Supporting Variants
Samples
Known GenesTMTC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691220
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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