A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265913



Internal ID20832953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:68883875..69126466hg38UCSC Ensembl
chr4:69749593..69992184hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38242592
hg19242592
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6569098
Supporting Variants
Samples
Known GenesUGT2A3, UGT2B10, UGT2B7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265913
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.01716


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