A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539022



Internal ID20912329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16868598..16877939hg38UCSC Ensembl
chr21:18240918..18250259hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg389342
hg199342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070960
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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