A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5860n54



Internal ID22773755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:12657196..12658192hg38UCSC Ensembl
chr18:12657195..12658191hg19UCSC Ensembl
chr18:12647195..12648191hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38997
hg19997
hg18997
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv576499, nsv576510, nsv576511
Samples
Known GenesSPIRE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5860n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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