A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534084



Internal ID20907445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5460102..5719171hg38UCSC Ensembl
chr20:5440748..5699817hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38259070
hg19259070
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4360n223
Supporting Variantsnssv18203256
Samples
Known GenesGPCPD1, LINC00654, LOC643406
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534084
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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