A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11225n54



Internal ID20144649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16868921..17375160hg38UCSC Ensembl
chr7:16908545..17414784hg19UCSC Ensembl
chr7:16875070..17381309hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38506240
hg19506240
hg18506240
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606342, nsv606340, nsv606341
SamplesHGDP01376
Known GenesAGR3, AHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11225n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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