A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512338



Internal ID15851763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:110934734..110937292hg38UCSC Ensembl
Outerchr13:111587081..111589639hg19UCSC Ensembl
Outerchr13:110385082..110387640hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382559
hg192559
hg182559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv624920
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512338
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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