A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14416991



Internal ID22152989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:76480065..76480065hg38UCSC Ensembl
chr13:77054201..77054201hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3549309
Supporting Variants
SamplesHG00514
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)nssv14416991
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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