A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642261



Internal ID7029031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38454372..38464818hg38UCSC Ensembl
Innerchr18:38454372..38464818hg38UCSC Ensembl
Outerchr18:38453872..38465318hg38UCSC Ensembl
chr18:36034336..36044782hg19UCSC Ensembl
Innerchr18:36034336..36044782hg19UCSC Ensembl
Outerchr18:36033836..36045282hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3810447
hg1910447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15844519
SamplesHG03567
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642261
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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