A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3545929



Internal ID22414930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38116157..38116157hg38UCSC Ensembl
chr20:36744559..36744559hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14394388
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)nsv3545929
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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