A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068397



Internal ID20635437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46666528..46705575hg38UCSC Ensembl
chr20:45295167..45334214hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3839048
hg1939048
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540438
Supporting Variants
Samples
Known GenesSLC13A3, TP53RK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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