A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676358



Internal ID9942463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26727641..26731153hg38UCSC Ensembl
Outerchr18:26727604..26731203hg38UCSC Ensembl
Innerchr18:24307605..24311117hg19UCSC Ensembl
Outerchr18:24307568..24311167hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5837086
SamplesHG00473
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676358
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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