A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264757



Internal ID20831797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143463455..143464378hg38UCSC Ensembl
chr4:144384608..144385531hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38924
hg19924
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571965
Supporting Variants
Samples
Known GenesGAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264757
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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