A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203908



Internal ID20770948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57325801..57353800hg38UCSC Ensembl
chr20:55900857..55928856hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg3828000
hg1928000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543017
Supporting Variants
Samples
Known GenesMIR5095, RAE1, SPO11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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