A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514862



Internal ID20888217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7434945..7475460hg38UCSC Ensembl
chr16:7484946..7525462hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3840516
hg1940517
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031404
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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