A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5985n223



Internal ID22808953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150093047..150093860hg38UCSC Ensembl
chr5:149472610..149473423hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38814
hg19814
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6564455, nsv6564990
Samples
Known GenesCSF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv5985n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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