A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203408



Internal ID20770448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62167075..62199737hg38UCSC Ensembl
chr20:60742131..60774793hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3832663
hg1932663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541228
Supporting Variants
Samples
Known GenesMTG2, SS18L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203408
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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