A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641932



Internal ID7028703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21126276..21131777hg38UCSC Ensembl
Innerchr18:21126326..21131727hg38UCSC Ensembl
Outerchr18:21126226..21131827hg38UCSC Ensembl
chr18:18706237..18711738hg19UCSC Ensembl
Innerchr18:18706287..18711688hg19UCSC Ensembl
Outerchr18:18706187..18711788hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15818607, essv15818606
SamplesHG02439, HG02332
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641932
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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