A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642075



Internal ID7028845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:29045139..29148226hg38UCSC Ensembl
Innerchr18:29045170..29148195hg38UCSC Ensembl
Outerchr18:29045108..29148257hg38UCSC Ensembl
chr18:26625103..26728191hg19UCSC Ensembl
Innerchr18:26625134..26728160hg19UCSC Ensembl
Outerchr18:26625072..26728222hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38103088
hg19103089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15830589
SamplesNA19452
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642075
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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