A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6518943



Internal ID20892304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5480803..5717463hg38UCSC Ensembl
chr20:5461449..5698109hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38236661
hg19236661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4360n223
Supporting Variantsnssv18203257
Samples
Known GenesGPCPD1, LINC00654
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6518943
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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