A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2233n152



Internal ID22817936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39352822..39352924hg38UCSC Ensembl
chr13:39926959..39927061hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3283615, nsv3285055
SamplesNA19240, HG00514
Known GenesLHFP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv2233n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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