A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18221720



Internal ID20788760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78072327..78073335hg38UCSC Ensembl
chr11:77783373..77784381hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381009
hg191009
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6591791
Supporting Variants
Samples
Known GenesNDUFC2, NDUFC2-KCTD14, RNU6-83P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18221720
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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