A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1183n145



Internal ID22814199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55202229..55209364hg38UCSC Ensembl
chr8:56114789..56121924hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg387136
hg197136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3116360, nsv3112352
Samplessample198, sample302, sample259
Known GenesXKR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv1183n145
Frequency
Sample Size467
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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