A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500188



Internal ID20873413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7712532..7791414hg38UCSC Ensembl
chr16:7762534..7841416hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3878883
hg1978883
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182067
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500188
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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