A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3089n223



Internal ID22806057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35638491..35640236hg38UCSC Ensembl
chr17:33965510..33967255hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381746
hg191746
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6587643, nsv6577071
Samples
Known GenesAP2B1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv3089n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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