A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11201n54



Internal ID22779096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10497229..10589304hg38UCSC Ensembl
chr7:10536856..10628931hg19UCSC Ensembl
chr7:10503381..10595456hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3892076
hg1992076
hg1892076
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606189, nsv606190
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11201n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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