A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213595



Internal ID22360493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43014865..43014962hg38UCSC Ensembl
chr15:43307063..43307160hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2908n152
Supporting Variantsnssv14430260
SamplesHG00514
Known GenesUBR1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213595
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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