A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7404468



Internal ID10682750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:26991656..26992377hg38UCSC Ensembl
Outerchr18:24571620..24572341hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3134901
Supporting Variants
SamplesHuRef
Known GenesCHST9
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7404468
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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