A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1119n145



Internal ID22814135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95711047..95733549hg38UCSC Ensembl
chr7:95340359..95362861hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3822503
hg1922503
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117369, nsv3112734
Samplessample90, sample15, sample404
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1119n145
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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