A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266431



Internal ID20833471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55862956..55863595hg38UCSC Ensembl
chr4:56729122..56729761hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38640
hg19640
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555856
Supporting Variants
Samples
Known GenesEXOC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266431
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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