A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496609



Internal ID20869812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86088832..86090137hg38UCSC Ensembl
chr16:86122438..86123743hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381306
hg191306
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191304
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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