A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11098n54



Internal ID20144522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:192140..193694hg38UCSC Ensembl
chr7:192140..193694hg19UCSC Ensembl
chr7:287223..288777hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381555
hg191555
hg181555
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv605624, nsv605629, nsv605627
Samples
Known GenesFAM20C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11098n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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