A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv472732



Internal ID15572160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170229727..170229727hg38UCSC Ensembl
chr4:171150878..171150878hg19UCSC Ensembl
chr4:171387453..171387453hg18UCSC Ensembl
chr4:171525608..171525608hg17UCSC Ensembl
Cytoband4q33
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 Variantsnssv3013990
SamplesNA18555
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)nsv472732
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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