A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538529



Internal ID20911843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:28561701..28569300hg38UCSC Ensembl
chr21:29934023..29941622hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538529
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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