A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508369



Internal ID20881668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63233201..63387700hg38UCSC Ensembl
chr16:63267105..63421604hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38154500
hg19154500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2904n223
Supporting Variantsnssv18181026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508369
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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