A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496455



Internal ID20869657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63492245..63581768hg38UCSC Ensembl
chr16:63526149..63615672hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3889524
hg1989524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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