A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14394466



Internal ID22289381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:42441738..42441738hg38UCSC Ensembl
chr2:42668878..42668878hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3537660
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)nssv14394466
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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