A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3654



Internal ID15201599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:46755700..46775645hg38UCSC Ensembl
Outerchr22:47151597..47171542hg19UCSC Ensembl
Outerchr22:45530261..45550206hg18UCSC Ensembl
Outerchr22:45472116..45492061hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg386462
hg196462
hg186462
hg176462
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5934
SamplesNA19129
Known GenesTBC1D22A
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)nsv3654
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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