A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2642n152



Internal ID22818345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63814886..63814947hg38UCSC Ensembl
chr14:64281604..64281665hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3212496, nsv3211646
SamplesHG00731, 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)dgv2642n152
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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