A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1005n145



Internal ID22814021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:269534..382543hg38UCSC Ensembl
chr6:269534..382543hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38113010
hg19113010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3110329, nsv3112774, nsv3117376
Samplessample303, sample402, sample130, sample302, sample275
Known GenesDUSP22
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1005n145
Frequency
Sample Size467
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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