A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536821



Internal ID20910164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26227801..26233400hg38UCSC Ensembl
chr21:27600120..27605719hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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