A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163823



Internal ID20730863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127952973..127962156hg38UCSC Ensembl
chr8:128965219..128974402hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg389184
hg199184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6433982
Supporting Variants
Samples
Known GenesMIR1205, PVT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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