A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504146



Internal ID20877407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87386104..87389074hg38UCSC Ensembl
chr16:87419710..87422680hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382971
hg192971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033621
Samples
Known GenesFBXO31
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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