A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv81n145



Internal ID22813097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:161531271..161673745hg38UCSC Ensembl
chr1:161501061..161643535hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38142475
hg19142475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3115991, nsv3114025, nsv3114593, nsv3117262
Samplessample196, sample83, sample365, sample369, sample404, sample43
Known GenesFCGR2B, FCGR2C, FCGR3A, FCGR3B, HSPA7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv81n145
Frequency
Sample Size467
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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