A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5395397



Internal ID8718856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:41284939..41287539hg38UCSC Ensembl
Innerchr18:38864903..38867503hg19UCSC Ensembl
Innerchr18:37118901..37121501hg18UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg382601
hg192601
hg182601
Variant TypeCNV loss
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656187
Supporting Variants
Samples2242 [59]
Known Genes
MethodMerging
AnalysisCalls merged from CNV Partition and PennCV algorithms
PlatformMerging
Comments
ReferenceChia_et_al_2012
Pubmed ID23635498
Accession Number(s)essv5395397
Frequency
Sample Size64
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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