A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11207n54



Internal ID22779102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12389177..12486656hg38UCSC Ensembl
chr7:12428803..12526282hg19UCSC Ensembl
chr7:12395328..12492807hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3897480
hg1997480
hg1897480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606226, nsv606227
Samples
Known GenesVWDE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11207n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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