A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3028n152



Internal ID22818731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92777677..92777773hg38UCSC Ensembl
chr15:93320907..93321003hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3529963, nsv3229460
SamplesNA19238, NA19239, NA19240
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv3028n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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