A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8745n152



Internal ID22824448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128316064..128316115hg38UCSC Ensembl
chr7:127956117..127956168hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3216478, nsv3222154
SamplesNA19238, NA19240
Known GenesRBM28
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)dgv8745n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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