A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641659



Internal ID7028433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5854544..5860407hg38UCSC Ensembl
Innerchr18:5854558..5860393hg38UCSC Ensembl
Outerchr18:5854530..5860421hg38UCSC Ensembl
chr18:5854543..5860406hg19UCSC Ensembl
Innerchr18:5854557..5860392hg19UCSC Ensembl
Outerchr18:5854529..5860420hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg385864
hg195864
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15792886, essv15792887
SamplesNA18998, NA18995
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641659
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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