A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9749915



Internal ID18724161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113802707..113803660hg38UCSC Ensembl
Outerchr13:113802568..113803766hg38UCSC Ensembl
Innerchr13:114505680..114506633hg19UCSC Ensembl
Outerchr13:114505541..114506739hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3551168
Supporting Variants
Samples
Known GenesTMEM255B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9749915
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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