A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3669



Internal ID15201615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:50475511..50509415hg38UCSC Ensembl
Outerchr22:50913940..50947844hg19UCSC Ensembl
Outerchr22:49260806..49294710hg18UCSC Ensembl
Outerchr22:49204084..49237988hg17UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg385531
hg195531
hg185531
hg175531
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7760
SamplesNA12156
Known GenesADM2, LMF2, MIOX, NCAPH2
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)nsv3669
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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