A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18269056



Internal ID20836096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:53667303..53668628hg38UCSC Ensembl
chr5:52963133..52964458hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg381326
hg191326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6574474
Supporting Variants
Samples
Known GenesNDUFS4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18269056
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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