A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6552440



Internal ID20925568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28714530..28743403hg38UCSC Ensembl
chr21:30086852..30115725hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3828874
hg1928874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206033
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6552440
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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