A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641864



Internal ID7028635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13928996..13944074hg38UCSC Ensembl
Innerchr18:13929031..13944040hg38UCSC Ensembl
Outerchr18:13928962..13944109hg38UCSC Ensembl
chr18:13928995..13944073hg19UCSC Ensembl
Innerchr18:13929030..13944039hg19UCSC Ensembl
Outerchr18:13928961..13944108hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3815079
hg1915079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15812717
SamplesHG03370
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641864
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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