A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3238n223



Internal ID22806206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:69513941..69514857hg38UCSC Ensembl
chr17:67510082..67510998hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6579798, nsv6594955
Samples
Known GenesMAP2K6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3238n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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