A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10818



Internal ID15195294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:55595175..55693085hg38UCSC Ensembl
Outerchr11:55362651..55460561hg19UCSC Ensembl
Outerchr11:55119227..55217137hg18UCSC Ensembl
Outerchr11:55119227..55217137hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3897911
hg1997911
hg1897911
hg1797911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv323
Supporting Variants
SamplesNA18956
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
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)nssv10818
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