A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3555249



Internal ID18756325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:37819739..37825776hg38UCSC Ensembl
Outerchr18:37819637..37825844hg38UCSC Ensembl
Innerchr18:35399703..35405740hg19UCSC Ensembl
Outerchr18:35399601..35405808hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg386208
hg196208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753996
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3555249
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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