A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7155n54



Internal ID20140579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165158204..165159737hg38UCSC Ensembl
chr2:166014714..166016247hg19UCSC Ensembl
chr2:165722960..165724493hg18UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg381534
hg191534
hg181534
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv583572, nsv583581, nsv583569, nsv583576, nsv583580, nsv583577, nsv583571, nsv583570
Samples
Known GenesSCN3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv7155n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss69
Observed Complex0
Frequencyn/a


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