A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641807



Internal ID7028578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11676947..11679170hg38UCSC Ensembl
Innerchr18:11676949..11679169hg38UCSC Ensembl
Outerchr18:11676946..11679172hg38UCSC Ensembl
chr18:11676946..11679169hg19UCSC Ensembl
Innerchr18:11676948..11679168hg19UCSC Ensembl
Outerchr18:11676945..11679171hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg382224
hg192224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15807336
SamplesHG01140
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641807
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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