A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv802n152



Internal ID22816505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12401141..12401317hg38UCSC Ensembl
chr10:12443140..12443316hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3226164, nsv3213891
SamplesNA19238, NA19240, HG00513
Known GenesCAMK1D
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)dgv802n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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