A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv176n152



Internal ID22815879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:31578440..31578606hg38UCSC Ensembl
chr1:32044041..32044207hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38167
hg19167
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3210342, nsv3203472
SamplesNA19238, NA19240
Known GenesTINAGL1
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)dgv176n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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