A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513080



Internal ID15852502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:141853145..141854921hg38UCSC Ensembl
Outerchr3:141571987..141573763hg19UCSC Ensembl
Outerchr3:143054677..143056453hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg381777
hg191777
hg181777
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv38n50
Supporting Variantsnssv626567
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)nsv513080
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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