A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2778n152



Internal ID22818481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:104905183..104905398hg38UCSC Ensembl
chr14:105371520..105371735hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38216
hg19216
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3225931, nsv3222566
SamplesNA19239, HG00731, HG00733
Known Genes
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)dgv2778n152
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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