A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753890



Internal ID18728136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:26167865..26170982hg38UCSC Ensembl
Outerchr18:26167730..26171427hg38UCSC Ensembl
Innerchr18:23747829..23750946hg19UCSC Ensembl
Outerchr18:23747694..23751391hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383698
hg193698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3555143
Supporting Variants
Samples
Known GenesPSMA8
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753890
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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