A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500795



Internal ID20874023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85987406..85989564hg38UCSC Ensembl
chr16:86021012..86023170hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382159
hg192159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181626
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500795
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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