A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642155



Internal ID7028925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:32540640..32615657hg38UCSC Ensembl
Innerchr18:32540641..32615656hg38UCSC Ensembl
Outerchr18:32540639..32615658hg38UCSC Ensembl
chr18:30120603..30195620hg19UCSC Ensembl
Innerchr18:30120604..30195619hg19UCSC Ensembl
Outerchr18:30120602..30195621hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3875018
hg1975018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15838107
SamplesHG03714
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642155
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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