A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641746



Internal ID7028517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9403994..9407374hg38UCSC Ensembl
Innerchr18:9403994..9407374hg38UCSC Ensembl
Outerchr18:9403815..9407543hg38UCSC Ensembl
chr18:9403992..9407372hg19UCSC Ensembl
Innerchr18:9403992..9407372hg19UCSC Ensembl
Outerchr18:9403813..9407541hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383381
hg193381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15800583
SamplesHG00246
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641746
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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