A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551442



Internal ID20924576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46320198..46321264hg38UCSC Ensembl
chr21:47740112..47741178hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381067
hg191067
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204206
Samples
Known GenesC21orf58
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551442
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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