A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642220



Internal ID6682301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36225645..36229282hg38UCSC Ensembl
Innerchr18:36225657..36229270hg38UCSC Ensembl
Outerchr18:36225633..36229294hg38UCSC Ensembl
chr18:33805608..33809245hg19UCSC Ensembl
Innerchr18:33805620..33809233hg19UCSC Ensembl
Outerchr18:33805596..33809257hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg383638
hg193638
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15842425
SamplesHG01947
Known GenesMOCOS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642220
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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