A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548864



Internal ID20922042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34012001..34015400hg38UCSC Ensembl
chr21:35384302..35387701hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383400
hg193400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4594n223
Supporting Variantsnssv18203923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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