A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218713



Internal ID22363971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95211312..95211369hg38UCSC Ensembl
chr15:95754541..95754598hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3037n152
Supporting Variantsnssv14405425
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218713
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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