A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641867



Internal ID7028638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14025638..14029777hg38UCSC Ensembl
Innerchr18:14025638..14029777hg38UCSC Ensembl
Outerchr18:14025462..14030074hg38UCSC Ensembl
chr18:14025637..14029776hg19UCSC Ensembl
Innerchr18:14025637..14029776hg19UCSC Ensembl
Outerchr18:14025461..14030073hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384140
hg194140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15812721, essv15812720
SamplesHG04202, HG03667
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641867
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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