A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6542246



Internal ID20915510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32016897..32017235hg38UCSC Ensembl
chr21:33389210..33389548hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18071918
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6542246
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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