A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204083



Internal ID20771123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:7582615..7594551hg38UCSC Ensembl
chr20:7563262..7575198hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3811937
hg1911937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6527812
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204083
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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