A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9376



Internal ID15193641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42116521..42141603hg38UCSC Ensembl
Outerchr22:42512525..42537613hg19UCSC Ensembl
Outerchr22:40842471..40867557hg18UCSC Ensembl
Outerchr22:40837025..40862111hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3825083
hg1925089
hg1825087
hg1725087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3641
Supporting Variants
SamplesNA18517
Known GenesCYP2D6, CYP2D7P, NDUFA6-AS1
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)nssv9376
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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