A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521078



Internal ID20894439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:30919401..30951500hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3832100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4436n223
Supporting Variantsnssv18202614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521078
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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