A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539819



Internal ID20913114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8685401..8693900hg38UCSC Ensembl
chr21:9574234..9582733hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4513n223
Supporting Variantsnssv18204237
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539819
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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