A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669185



Internal ID9935290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:9043813..9047285hg38UCSC Ensembl
Outerchr18:9043776..9047335hg38UCSC Ensembl
Innerchr18:9043811..9047283hg19UCSC Ensembl
Outerchr18:9043774..9047333hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg383560
hg193560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv581e199
Supporting Variantsessv5941465
SamplesNA20536
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669185
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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