A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv473194



Internal ID15572624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57536803..57536803hg38UCSC Ensembl
chr11:57304276..57304276hg19UCSC Ensembl
chr11:57060852..57060852hg18UCSC Ensembl
chr11:57060852..57060852hg17UCSC Ensembl
Cytoband11q12.1
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 Variantsnssv3020227
SamplesNA19129
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)nsv473194
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