A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5883n152



Internal ID22821586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15592526..15592677hg38UCSC Ensembl
chr3:15634033..15634184hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3280227, nsv3280297
SamplesNA19240, HG00514
Known GenesHACL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv5883n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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