A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642710



Internal ID7029479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:60665234..60721951hg38UCSC Ensembl
Innerchr18:60665234..60721951hg38UCSC Ensembl
Outerchr18:60664734..60722451hg38UCSC Ensembl
chr18:58332467..58389184hg19UCSC Ensembl
Innerchr18:58332467..58389184hg19UCSC Ensembl
Outerchr18:58331967..58389684hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg3856718
hg1956718
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv618e214
Supporting Variantsessv15898527
SamplesHG00472
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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