A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2673n223



Internal ID22805641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6843858..7030800hg38UCSC Ensembl
chr16:6893859..7080801hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38186943
hg19186943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6502009, nsv6510802
Samples
Known GenesRBFOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv2673n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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