A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv979n145



Internal ID22813995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82657316..82659010hg38UCSC Ensembl
chr5:81953135..81954829hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg381695
hg191695
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111807, nsv3112390
Samplessample38, sample312, sample140, sample300, sample111, sample231, sample172
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv979n145
Frequency
Sample Size467
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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