A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12474n54



Internal ID22780369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2148877..2150862hg38UCSC Ensembl
chr9:2148877..2150862hg19UCSC Ensembl
chr9:2138877..2140862hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg381986
hg191986
hg181986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613105, nsv613112, nsv613104, nsv613115
Samples
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12474n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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