A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642228



Internal ID6682309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36409033..36411111hg38UCSC Ensembl
Innerchr18:36409083..36411061hg38UCSC Ensembl
Outerchr18:36408983..36411161hg38UCSC Ensembl
chr18:33988996..33991074hg19UCSC Ensembl
Innerchr18:33989046..33991024hg19UCSC Ensembl
Outerchr18:33988946..33991124hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg382079
hg192079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842435
SamplesHG00245
Known GenesFHOD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642228
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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