A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265153



Internal ID20832193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39479436..39479650hg38UCSC Ensembl
chr4:39481056..39481270hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571730
Supporting Variants
Samples
Known GenesMIR1273H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265153
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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