A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10123n54



Internal ID22778018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151410812..151413016hg38UCSC Ensembl
chr5:150790373..150792577hg19UCSC Ensembl
chr5:150770566..150772770hg18UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg382205
hg192205
hg182205
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv600014, nsv600029, nsv600022, nsv600025, nsv600030, nsv600013
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10123n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss130
Observed Complex0
Frequencyn/a


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