A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12475n54



Internal ID22780370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2148877..2151371hg38UCSC Ensembl
chr9:2148877..2151371hg19UCSC Ensembl
chr9:2138877..2141371hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg382495
hg192495
hg182495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv613113, nsv613109, nsv613110, nsv613116, nsv613106, nsv613107
Samples
Known GenesSMARCA2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12475n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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