A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501096



Internal ID20874327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77893031..78561479hg38UCSC Ensembl
chr16:77926928..78595376hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38668449
hg19668449
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2942n223
Supporting Variantsnssv18177746
Samples
Known GenesCLEC3A, VAT1L, WWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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