A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642304



Internal ID7029074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40705072..40709722hg38UCSC Ensembl
Innerchr18:40705081..40709714hg38UCSC Ensembl
Outerchr18:40705064..40709731hg38UCSC Ensembl
chr18:38285036..38289686hg19UCSC Ensembl
Innerchr18:38285045..38289678hg19UCSC Ensembl
Outerchr18:38285028..38289695hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg384651
hg194651
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15849367
SamplesHG01863
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642304
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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