A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17044046



Internal ID97097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33045369..33049250hg38UCSC Ensembl
chr11:33066915..33070796hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg383882
hg193882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5506822
Supporting Variants
Samples
Known GenesTCP11L1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17044046
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