A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17590064



Internal ID21782107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81275717..81276559hg38UCSC Ensembl
chr8:82187952..82188794hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005932
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17590064
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