A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675696



Internal ID9941801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:1196671..1885547hg38UCSC Ensembl
Outerchr18:1196637..1885582hg38UCSC Ensembl
Innerchr18:1196672..1885548hg19UCSC Ensembl
Outerchr18:1196638..1885583hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38688946
hg19688946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5532232
SamplesNA19248
Known GenesLINC00470
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675696
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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