A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226771



Internal ID20793811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77858342..77859188hg38UCSC Ensembl
chr10:79618100..79618946hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38847
hg19847
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6582442
Supporting Variants
Samples
Known GenesDLG5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226771
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00012


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