A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1065n145



Internal ID22814081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:119076451..119080240hg38UCSC Ensembl
chr6:119397616..119401405hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg383790
hg193790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111800, nsv3110790
Samplessample349, sample139
Known GenesFAM184A
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1065n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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