A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217579



Internal ID20784619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101107659..101111032hg38UCSC Ensembl
chr10:102867416..102870789hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg383374
hg193374
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579072
Supporting Variants
Samples
Known GenesTLX1NB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217579
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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