A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555490



Internal ID18756566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61518413..61521812hg38UCSC Ensembl
Outerchr18:61518272..61521849hg38UCSC Ensembl
Innerchr18:59185646..59189045hg19UCSC Ensembl
Outerchr18:59185505..59189082hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383578
hg193578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9754237
Samples
Known GenesCDH20
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555490
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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