A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6469



Internal ID15190709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:74424817..74470372hg38UCSC Ensembl
Outerchr11:74135862..74181417hg19UCSC Ensembl
Outerchr11:73813510..73859065hg18UCSC Ensembl
Outerchr11:73813510..73859065hg17UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3845556
hg1945556
hg1845556
hg1745556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv393
Supporting Variants
SamplesNA12156
Known GenesKCNE3
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)nssv6469
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