A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9767n152



Internal ID22825470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132378505..132378618hg38UCSC Ensembl
chr9:135253892..135254005hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3527502, nsv3223655
SamplesHG00512, NA19238, NA19239, NA19240
Known GenesTTF1
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)dgv9767n152
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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