A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386162



Internal ID22309698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14514372..14514372hg38UCSC Ensembl
chr1:14840868..14840868hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3537370
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)nssv14386162
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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