A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10130n54



Internal ID22778025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152133822..152148270hg38UCSC Ensembl
chr5:151513383..151527831hg19UCSC Ensembl
chr5:151493576..151508024hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3814449
hg1914449
hg1814449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600063, nsv600045
Samples1780854205_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10130n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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