A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3541543



Internal ID22410641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12774615..12774615hg38UCSC Ensembl
chr8:12632124..12632124hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14428054
SamplesHG00514
Known GenesLOC340357
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)nsv3541543
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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