A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535720



Internal ID20909074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41664045..41664681hg38UCSC Ensembl
chr21:43084205..43084841hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071539
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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