A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558148



Internal ID20931219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:69206932..69416699hg38UCSC Ensembl
chr4:70072650..70282417hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38209768
hg19209768
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5317n223
Supporting Variantsnssv18265918
Samples
Known GenesUGT2B11, UGT2B28
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558148
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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