A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264946



Internal ID20831986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166047237..166048142hg38UCSC Ensembl
chr4:166968389..166969294hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6558762
Supporting Variants
Samples
Known GenesTLL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264946
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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