A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068869



Internal ID20635909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38865900..38867314hg38UCSC Ensembl
chr20:37494543..37495957hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg381415
hg191415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6530384
Supporting Variants
Samples
Known GenesPPP1R16B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068869
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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