A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205873



Internal ID20772913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:52477448..52505957hg38UCSC Ensembl
chr20:51093987..51122496hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3828510
hg1928510
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553870
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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