A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1066n145



Internal ID22814082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120657040..120687561hg38UCSC Ensembl
chr6:120978186..121008707hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3830522
hg1930522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114202, nsv3117130
Samplessample379, sample420, sample101, sample205, sample35
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1066n145
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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