A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554971



Internal ID18409361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3635367..3636951hg38UCSC Ensembl
Outerchr18:3635321..3636963hg38UCSC Ensembl
Innerchr18:3635366..3636950hg19UCSC Ensembl
Outerchr18:3635320..3636962hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381643
hg191643
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753718
Samples
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554971
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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