A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3286664



Internal ID22385056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:35656384..35656511hg38UCSC Ensembl
chr15:35948585..35948712hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38128
hg19128
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14404588
SamplesNA19240
Known GenesDPH6-AS1
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)nsv3286664
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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