A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264114



Internal ID20831154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139298190..139299121hg38UCSC Ensembl
chr4:140219344..140220275hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38932
hg19932
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561732
Supporting Variants
Samples
Known GenesNDUFC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0002


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