A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539651



Internal ID20912947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:45807089..45817223hg38UCSC Ensembl
chr21:47227003..47237137hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810135
hg1910135
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204183
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539651
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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