A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17438774



Internal ID22496644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:133114608..133114692hg38UCSC Ensembl
chr8:134126852..134126936hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917534
Supporting Variants
Samples
Known GenesTG
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17438774
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