A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18227780



Internal ID20794820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:113762246..113762365hg38UCSC Ensembl
chr10:115522005..115522124hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584006
Supporting Variants
Samples
Known GenesPLEKHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18227780
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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