A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3238n152



Internal ID22818941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58993695..58994252hg38UCSC Ensembl
chr16:59027599..59028156hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38558
hg19558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3528841, nsv3285149
SamplesHG00512, NA19239, NA19240
Known Genes
MethodMerging
Sequencing
AnalysisMultiple analysis algorthms
PhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformIllumina HiSeq
See merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)dgv3238n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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