A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268949



Internal ID20835989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60990389..60991318hg38UCSC Ensembl
chr5:60286216..60287145hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568070
Supporting Variants
Samples
Known GenesNDUFAF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268949
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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