A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505186



Internal ID20878452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86464172..86464712hg38UCSC Ensembl
chr16:86497778..86498318hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38541
hg19541
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177795
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505186
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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