A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524598



Internal ID20897959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:8917919..9087644hg38UCSC Ensembl
chr20:8898566..9068291hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg38169726
hg19169726
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202997
Samples
Known GenesPLCB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524598
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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