A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203880



Internal ID20770920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5588564..5648375hg38UCSC Ensembl
chr20:5569210..5629021hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3859812
hg1959812
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516685
Supporting Variants
Samples
Known GenesGPCPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203880
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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