A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14394345



Internal ID22286218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:29410408..29410408hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381372
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3547500
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14394345
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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