A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5871n54



Internal ID22773766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:15390016..15408106hg38UCSC Ensembl
chr18:15390015..15408105hg19UCSC Ensembl
chr18:15380015..15398105hg18UCSC Ensembl
Cytoband18p11.1
Allele length
AssemblyAllele length
hg3818091
hg1918091
hg1818091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576558, nsv576559
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5871n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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