A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11054



Internal ID15192968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36744915..36794250hg38UCSC Ensembl
Outerchr22:37140959..37190294hg19UCSC Ensembl
Outerchr22:35470905..35520240hg18UCSC Ensembl
Outerchr22:35465459..35514794hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3849336
hg1949336
hg1849336
hg1749336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3617
Supporting Variants
SamplesNA15510
Known GenesIFT27
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)nssv11054
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