A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066985



Internal ID20634025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19219959..19222109hg38UCSC Ensembl
chr20:19200603..19202753hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534641
Supporting Variants
Samples
Known GenesSLC24A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066985
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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