A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18230611



Internal ID20797651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:635864..731287hg38UCSC Ensembl
chr10:681804..777227hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3895424
hg1995424
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592826
Supporting Variants
Samples
Known GenesDIP2C, MIR5699, PRR26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18230611
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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