A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203439



Internal ID20770479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63505575..63542048hg38UCSC Ensembl
chr20:62136928..62173401hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3836474
hg1936474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537120
Supporting Variants
Samples
Known GenesPPDPF, PTK6, SRMS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203439
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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