A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11489n54



Internal ID22779384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87697613..87723256hg38UCSC Ensembl
chr7:87326929..87352572hg19UCSC Ensembl
chr7:87164865..87190508hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3825644
hg1925644
hg1825644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607729, nsv607730
Samples
Known GenesABCB1, RUNDC3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11489n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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