A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1105n145



Internal ID22814121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:49768904..49775121hg38UCSC Ensembl
chr7:49808500..49814717hg19UCSC Ensembl
Cytoband7p12.2
Allele length
AssemblyAllele length
hg386218
hg196218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3117080, nsv3114915
Samplessample348, sample353
Known GenesVWC2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1105n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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