A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10132n54



Internal ID22778027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:152134610..152145586hg38UCSC Ensembl
chr5:151514171..151525147hg19UCSC Ensembl
chr5:151494364..151505340hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3810977
hg1910977
hg1810977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600061, nsv600050, nsv600082, nsv600071, nsv600062
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10132n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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