A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514864



Internal ID20888219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84560762..84562805hg38UCSC Ensembl
chr16:84594368..84596411hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382044
hg192044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179172
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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