A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642238



Internal ID6682319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36673097..36679908hg38UCSC Ensembl
Innerchr18:36673097..36679908hg38UCSC Ensembl
Outerchr18:36672876..36680145hg38UCSC Ensembl
chr18:34253060..34259871hg19UCSC Ensembl
Innerchr18:34253060..34259871hg19UCSC Ensembl
Outerchr18:34252839..34260108hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386812
hg196812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842463
SamplesNA18505
Known GenesFHOD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642238
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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