A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18266333



Internal ID20833373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:46887675..46888467hg38UCSC Ensembl
chr4:46889692..46890484hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg38793
hg19793
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571752
Supporting Variants
Samples
Known GenesCOX7B2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18266333
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00028


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