A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv335



Internal ID15201264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:59919816..59954469hg38UCSC Ensembl
Outerchr11:59687289..59721942hg19UCSC Ensembl
Outerchr11:59443865..59478518hg18UCSC Ensembl
Outerchr11:59443865..59478518hg17UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg385376
hg195376
hg185376
hg175376
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2868
SamplesNA18555
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv335
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