A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18239173



Internal ID20806213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19080079..19083558hg38UCSC Ensembl
chr16:19091401..19094880hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg383480
hg193480
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6594100
Supporting Variants
Samples
Known GenesCOQ7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18239173
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00036


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