A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3199n223



Internal ID22806167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:58477412..58478166hg38UCSC Ensembl
chr17:56554773..56555527hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38755
hg19755
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577491, nsv6581077
Samples
Known GenesHSF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3199n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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