A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv308n152



Internal ID22816011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83892229..83892309hg38UCSC Ensembl
chr1:84357912..84357992hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3195823, nsv3200800
SamplesHG00512, HG00514
Known GenesMIR548AP, TTLL7
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)dgv308n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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