A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642267



Internal ID7029037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38697238..38733271hg38UCSC Ensembl
Innerchr18:38697238..38733271hg38UCSC Ensembl
Outerchr18:38696738..38733771hg38UCSC Ensembl
chr18:36277202..36313235hg19UCSC Ensembl
Innerchr18:36277202..36313235hg19UCSC Ensembl
Outerchr18:36276702..36313735hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3836034
hg1936034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15844633
SamplesHG01345
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642267
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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