A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380889



Internal ID22286068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103992732..103992841hg38UCSC Ensembl
chr10:105752490..105752599hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201758
Supporting Variants
SamplesNA19240
Known GenesSLK
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380889
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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