A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264185



Internal ID20831225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118694933..118695292hg38UCSC Ensembl
chr4:119616088..119616447hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556896
Supporting Variants
Samples
Known GenesMETTL14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264185
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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