A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9351n152



Internal ID22825054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132028544..132028618hg38UCSC Ensembl
chr8:133040791..133040865hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3529213, nsv3287875, nsv3287900
SamplesNA19239, NA19240, HG00733
Known GenesOC90
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)dgv9351n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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