A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662406



Internal ID9581825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3635448..3638228hg38UCSC Ensembl
Outerchr18:3635411..3638278hg38UCSC Ensembl
Innerchr18:3635447..3638227hg19UCSC Ensembl
Outerchr18:3635410..3638277hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg382868
hg192868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6596313
SamplesNA19213
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662406
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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