A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14389433



Internal ID22297693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110360256..110360256hg38UCSC Ensembl
chr10:112120014..112120014hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3547013
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14389433
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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