A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513039



Internal ID15852461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:27092695..27093727hg38UCSC Ensembl
Outerchr3:27134186..27135218hg19UCSC Ensembl
Outerchr3:27109190..27110222hg18UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg381033
hg191033
hg181033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626522
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)nsv513039
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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