A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203207



Internal ID20770247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20709901..20715200hg38UCSC Ensembl
chr20:20690544..20695843hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6521971
Supporting Variants
Samples
Known GenesRALGAPA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203207
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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