A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525554



Internal ID20898915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2778405..2808128hg38UCSC Ensembl
chr20:2759051..2788774hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829724
hg1929724
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202569
Samples
Known GenesCPXM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525554
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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