A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511680



Internal ID20885010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7123587..7155253hg38UCSC Ensembl
chr16:7173588..7205254hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3831667
hg1931667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031936
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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