A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv978n145



Internal ID22813994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65880717..65888683hg38UCSC Ensembl
chr5:65176545..65184511hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg387967
hg197967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114216, nsv3114764
Samplessample141, sample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv978n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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