A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519999



Internal ID20893360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38362100..38394726hg38UCSC Ensembl
chr20:36990754..37023368hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3832627
hg1932615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202239
Samples
Known GenesLBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519999
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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