A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526096



Internal ID20899457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:25453191..25613232hg38UCSC Ensembl
chr20:25433827..25593868hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38160042
hg19160042
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202562
Samples
Known GenesNANP, NINL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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