A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1122n145



Internal ID22814138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106109961..106114077hg38UCSC Ensembl
chr7:105750407..105754523hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg384117
hg194117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3114064, nsv3110846
Samplessample349, sample348
Known GenesSYPL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1122n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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