A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4051n152



Internal ID22819754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1005741..1006147hg38UCSC Ensembl
chr19:1005740..1006146hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3210757, nsv3230329
SamplesNA19238, HG00733
Known GenesGRIN3B
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)dgv4051n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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