A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067971



Internal ID20635011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34877493..34880382hg38UCSC Ensembl
chr20:33465296..33468185hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg382890
hg192890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526259
Supporting Variants
Samples
Known GenesACSS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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