A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264394



Internal ID20831434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169742839..169743351hg38UCSC Ensembl
chr4:170663990..170664502hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562706
Supporting Variants
Samples
Known GenesC4orf27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264394
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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