A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6522420



Internal ID20895781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:13413087..13829468hg38UCSC Ensembl
chr20:13393734..13810114hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38416382
hg19416381
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202177
Samples
Known GenesESF1, NDUFAF5, TASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6522420
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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