A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551182



Internal ID20924319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40921851..40928169hg38UCSC Ensembl
chr21:42293777..42300095hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg386319
hg196319
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551182
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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