A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529367



Internal ID20902728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:33058105..33061162hg38UCSC Ensembl
chr20:31645911..31648968hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg383058
hg193058
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203283
Samples
Known GenesBPIFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529367
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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