A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9754238



Internal ID18728484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:61616655..61616862hg38UCSC Ensembl
Outerchr18:61616619..61616900hg38UCSC Ensembl
Innerchr18:59283888..59284095hg19UCSC Ensembl
Outerchr18:59283852..59284133hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555491
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9754238
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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