A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594654



Internal ID21786697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95074413..95074555hg38UCSC Ensembl
chr8:96086641..96086783hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003498
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594654
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