A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515244



Internal ID20888603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:5721115..6072259hg38UCSC Ensembl
chr16:5771116..6122260hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38351145
hg19351145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029776
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515244
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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