A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513065



Internal ID15852487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:107318516..107321492hg38UCSC Ensembl
Outerchr3:107037363..107040339hg19UCSC Ensembl
Outerchr3:108520053..108523029hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382977
hg192977
hg182977
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626550
Samples1
Known GenesLINC00883
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513065
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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