A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749852



Internal ID18724098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111670758..111670849hg38UCSC Ensembl
chr13:112323105..112323196hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551105
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749852
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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