A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068998



Internal ID20636038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4950651..4991329hg38UCSC Ensembl
chr20:4931297..4971975hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3840679
hg1940679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6525891
Supporting Variants
Samples
Known GenesSLC23A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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