A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6562n152



Internal ID22822265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40633687..40635776hg38UCSC Ensembl
chr4:40635704..40637793hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382090
hg192090
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3201752, nsv3201642
SamplesNA19239
Known Genes
MethodOptical mapping
Sequencing
AnalysisBioNano Genomics proprietary analysis
Multiple analysis algorthms
PlatformBioNano Genomics
Illumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv6562n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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