A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10241n54



Internal ID20143665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179794788..179802039hg38UCSC Ensembl
chr5:179221789..179229039hg19UCSC Ensembl
chr5:179154395..179161645hg18UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg387252
hg197251
hg187251
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600667, nsv600663, nsv600664
Samples
Known GenesLTC4S, MGAT4B, MIR1229
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10241n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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