A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11226n54



Internal ID22779121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:17360234..17589927hg38UCSC Ensembl
chr7:17399858..17629551hg19UCSC Ensembl
chr7:17366383..17596076hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38229694
hg19229694
hg18229694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606347, nsv606348, nsv606346
SamplesNINDS_165, 1782681286_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11226n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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