A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525076



Internal ID20898437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30627601..30642300hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3814700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4432n223
Supporting Variantsnssv18202601
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525076
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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