A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv495



Internal ID15549710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:112663378..112692830hg38UCSC Ensembl
Outerchr11:112534101..112563553hg19UCSC Ensembl
Outerchr11:112039311..112068763hg18UCSC Ensembl
Outerchr11:112039311..112068763hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3829453
hg1929453
hg1829453
hg1729453
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1964
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)nsv495
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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