A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14442694



Internal ID22228690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:87926230..87926697hg38UCSC Ensembl
chr10:89685987..89686454hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38468
hg19468
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193080
Supporting Variants
SamplesHG00733
Known GenesPTEN
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14442694
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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