A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203263



Internal ID20770303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:318748..687991hg38UCSC Ensembl
chr20:299392..668635hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38369244
hg19369244
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516354
Supporting Variants
Samples
Known GenesCSNK2A1, NRSN2, RBCK1, SCRT2, SOX12, SRXN1, TBC1D20, TCF15, TRIB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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