A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264830



Internal ID20831870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148220176..148220598hg38UCSC Ensembl
chr4:149141327..149141749hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574151
Supporting Variants
Samples
Known GenesNR3C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264830
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00028


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