A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3642



Internal ID15201586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42115497..42128296hg38UCSC Ensembl
Outerchr22:42511501..42524298hg19UCSC Ensembl
Outerchr22:40841447..40854242hg18UCSC Ensembl
Outerchr22:40836001..40848796hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3811582
hg1911582
hg1811582
hg1711582
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9872, nssv2377
SamplesNA18507, NA18555
Known GenesCYP2D6, 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)nsv3642
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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