A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641769



Internal ID7028540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10279529..10289114hg38UCSC Ensembl
Innerchr18:10279679..10288964hg38UCSC Ensembl
Outerchr18:10279379..10289264hg38UCSC Ensembl
chr18:10279526..10289111hg19UCSC Ensembl
Innerchr18:10279676..10288961hg19UCSC Ensembl
Outerchr18:10279376..10289261hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg389586
hg199586
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15804424
SamplesHG03100
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641769
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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