A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166604



Internal ID20733644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:33179187..33180591hg38UCSC Ensembl
chr8:33036705..33038109hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg381405
hg191405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418935
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00102


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