A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3554148



Internal ID22423016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70376568..70376568hg38UCSC Ensembl
chr15:70668907..70668907hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14382423
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)nsv3554148
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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