A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1042n145



Internal ID22814058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:71600730..71604403hg38UCSC Ensembl
chr6:72310433..72314106hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg383674
hg193674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114887, nsv3116240, nsv3114048
Samplessample146, sample218, sample14
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1042n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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