A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505724



Internal ID20878997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5530830..5971638hg38UCSC Ensembl
chr16:5580831..6021639hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38440809
hg19440809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190876
Samples
Known GenesMIR8065
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505724
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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