A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355373



Internal ID22581042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44915324..44918966hg38UCSC Ensembl
chr10:45410772..45414414hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg383643
hg193643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5911791
Supporting Variants
Samples
Known GenesTMEM72, TMEM72-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355373
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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