A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527893



Internal ID20901254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24327394..24331582hg38UCSC Ensembl
chr20:24308030..24312218hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg384189
hg194189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527893
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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