A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3626n152



Internal ID22819329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71161944..71162002hg38UCSC Ensembl
chr17:69158085..69158143hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3225986, nsv3213959
SamplesNA19240
Known GenesCASC17
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)dgv3626n152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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