A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626717



Internal ID15850250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:2861129..2863467hg38UCSC Ensembl
Outerchr5:2861243..2863581hg19UCSC Ensembl
Outerchr5:2914243..2916581hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382339
hg192339
hg182339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513215
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)nssv626717
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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