A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223214



Internal ID20790254
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76145384..76476433hg38UCSC Ensembl
chr10:77905142..78236191hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38331050
hg19331050
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576248
Supporting Variants
Samples
Known GenesC10orf11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223214
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00041


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