A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9750n152



Internal ID22825453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126484534..126485603hg38UCSC Ensembl
chr9:129246813..129247882hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381070
hg191070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3219018, nsv3529079
SamplesNA19238, NA19239, HG00732, NA19240
Known GenesMVB12B
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)dgv9750n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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