A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17597457



Internal ID21789500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87530719..87546978hg38UCSC Ensembl
chr8:88542947..88559206hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3816260
hg1916260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016440
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17597457
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