A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642087



Internal ID7028857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29629729..29646295hg38UCSC Ensembl
Innerchr18:29629753..29646272hg38UCSC Ensembl
Outerchr18:29629706..29646319hg38UCSC Ensembl
chr18:27209694..27226260hg19UCSC Ensembl
Innerchr18:27209718..27226237hg19UCSC Ensembl
Outerchr18:27209671..27226284hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3816567
hg1916567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15832782
SamplesHG03199
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642087
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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