A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6007n223



Internal ID22808975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162009971..162012683hg38UCSC Ensembl
chr5:161436977..161439689hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg382713
hg192713
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6574118, nsv6571165
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv6007n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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