A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666773



Internal ID9586192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3635433..3637001hg38UCSC Ensembl
Outerchr18:3635396..3637051hg38UCSC Ensembl
Innerchr18:3635432..3637000hg19UCSC Ensembl
Outerchr18:3635395..3637050hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv578e199
Supporting Variantsessv5613962
SamplesHG00702
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666773
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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