A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3287326



Internal ID22385729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71286489..71286603hg38UCSC Ensembl
chr11:70997535..70997649hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14379286
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)nsv3287326
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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