A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6478



Internal ID15537385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:101674990..101713273hg38UCSC Ensembl
Outerchr11:101545721..101584004hg19UCSC Ensembl
Outerchr11:101050931..101089214hg18UCSC Ensembl
Outerchr11:101050931..101089214hg17UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3838284
hg1938284
hg1838284
hg1738284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv461
Supporting Variants
SamplesNA12156
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)nssv6478
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