A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv106n145



Internal ID22813122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202738070..202741545hg38UCSC Ensembl
chr1:202707198..202710673hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg383476
hg193476
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3118049, nsv3115201
Samplessample361, sample96
Known GenesKDM5B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv106n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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