A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626552



Internal ID15850085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:113024234..113033750hg38UCSC Ensembl
Outerchr3:112743081..112752597hg19UCSC Ensembl
Outerchr3:114225771..114235287hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg389517
hg199517
hg189517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513067
Supporting Variants
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)nssv626552
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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