A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624927



Internal ID15501777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:113802577..113803700hg38UCSC Ensembl
Outerchr13:114505550..114506673hg19UCSC Ensembl
Outerchr13:113607270..113608393hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381124
hg191124
hg181124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512344
Supporting Variants
Samples1
Known GenesTMEM255B
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624927
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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