A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1097n145



Internal ID22814113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16309237..16362465hg38UCSC Ensembl
chr7:16348862..16402090hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3853229
hg1953229
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117141, nsv3117070, nsv3110405
Samplessample396, sample271, sample412, sample343, sample302, sample89, sample86
Known GenesISPD
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1097n145
Frequency
Sample Size467
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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