A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512928



Internal ID15852350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138650748..138650833hg38UCSC Ensembl
Outerchr7:138335493..138335578hg19UCSC Ensembl
Outerchr7:137986033..137986118hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381310
hg191310
hg181310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625576
Samples1
Known GenesSVOPL
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512928
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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