A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6233n152



Internal ID22821936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163237261..163314344hg38UCSC Ensembl
chr3:162955049..163032132hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3877084
hg1977084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3202908, nsv3197229
SamplesNA19240
Known GenesCT64
MethodMerging
Optical mapping
AnalysisBioNano Genomics proprietary analysis
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformBioNano Genomics
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6233n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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