A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519638



Internal ID20892999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32280685..32281602hg38UCSC Ensembl
chr20:30868488..30869405hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203272
Samples
Known GenesKIF3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519638
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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