A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3287327



Internal ID22385730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25966883..25966994hg38UCSC Ensembl
chr15:26212030..26212141hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2855n152
Supporting Variantsnssv14405744
SamplesNA19240
Known GenesLOC100128714
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)nsv3287327
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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