A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642052



Internal ID6682133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:28025186..28026338hg38UCSC Ensembl
Innerchr18:28025189..28026335hg38UCSC Ensembl
Outerchr18:28025183..28026341hg38UCSC Ensembl
chr18:25605150..25606302hg19UCSC Ensembl
Innerchr18:25605153..25606299hg19UCSC Ensembl
Outerchr18:25605147..25606305hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381153
hg191153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15827258
SamplesNA18603
Known GenesCDH2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642052
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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