A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv479039



Internal ID15578465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85676301..85676301hg38UCSC Ensembl
chr6:86386019..86386019hg19UCSC Ensembl
chr6:86442738..86442738hg18UCSC Ensembl
chr6:86442738..86442738hg17UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3012253
Samples
Known Genes
MethodSequencing
AnalysisSearch fosmid ESPs as described in Tuzun et al (2005)
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA singleton. The coordinate provided is from the mappable member of a fosmid end sequence pair, and indicates the genomic vicinity of a novel sequence insertion
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nsv479039
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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