A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv966n223



Internal ID22803934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7017624..7018645hg38UCSC Ensembl
chr11:7038855..7039876hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381022
hg191022
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6577393, nsv6589354
Samples
Known GenesZNF214
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv966n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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