A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3283922



Internal ID22382278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68133679..68136603hg38UCSC Ensembl
chr15:68426017..68428941hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382925
hg192925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2967n152
Supporting Variantsnssv14462395
SamplesHG00733
Known GenesPIAS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences detected as low complexity by RepeatMasker/3.3.0
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3283922
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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