A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498880



Internal ID20872094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6938908..7070609hg38UCSC Ensembl
chr16:6988909..7120610hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38131702
hg19131702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031789
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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