A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5862n152



Internal ID22821565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8410884..8413654hg38UCSC Ensembl
chr3:8452570..8455340hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382771
hg192771
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3174174, nsv3174034
SamplesNA19240, HG00733
Known GenesLMCD1-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv5862n152
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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