A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497878



Internal ID20871086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56735415..57030364hg38UCSC Ensembl
chr16:56769327..57064276hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38294950
hg19294950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196646
Samples
Known GenesCETP, HERPUD1, MIR138-2, MIR6863, NLRC5, NUP93, SLC12A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497878
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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