A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5913n54



Internal ID22773808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44397449..44401251hg38UCSC Ensembl
chr18:41977414..41981216hg19UCSC Ensembl
chr18:40231412..40235214hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg383803
hg193803
hg183803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576793, nsv576798, nsv576794, nsv576797
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5913n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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