A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232355



Internal ID20799395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87908710..87909269hg38UCSC Ensembl
chr10:89668467..89669026hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6577676
Supporting Variants
Samples
Known GenesPTEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232355
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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