A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173072



Internal ID20740112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89724301..89728700hg38UCSC Ensembl
chr8:90736529..90740928hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434440
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00565


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