A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067775



Internal ID20634815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:43562443..43563135hg38UCSC Ensembl
chr20:42191083..42191775hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549236
Supporting Variants
Samples
Known GenesSGK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067775
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