A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv474861



Internal ID15574293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:55578599..55578599hg38UCSC Ensembl
chr20:54153657..54153657hg19UCSC Ensembl
chr20:53587064..53587064hg18UCSC Ensembl
chr20:53587064..53587064hg17UCSC Ensembl
Cytoband20q13.2
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 Variantsnssv3018510
SamplesNA18956
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)nsv474861
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer