A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642395



Internal ID7029165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:44403962..44431111hg38UCSC Ensembl
Innerchr18:44403962..44431111hg38UCSC Ensembl
Outerchr18:44403462..44431611hg38UCSC Ensembl
chr18:41983927..42011076hg19UCSC Ensembl
Innerchr18:41983927..42011076hg19UCSC Ensembl
Outerchr18:41983427..42011576hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3827150
hg1927150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15856901
SamplesHG00111
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642395
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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