A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203422



Internal ID20770462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62838963..62848776hg38UCSC Ensembl
chr20:61470315..61480128hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg389814
hg199814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541478
Supporting Variants
Samples
Known GenesCOL9A3, DPH3P1, TCFL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203422
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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