A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10327



Internal ID15195785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42140023..42163392hg38UCSC Ensembl
Outerchr22:42536034..42559398hg19UCSC Ensembl
Outerchr22:40865978..40889342hg18UCSC Ensembl
Outerchr22:40860532..40883896hg17UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3816138
hg1916138
hg1816138
hg1716138
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3643
Supporting Variants
SamplesNA18956
Known GenesCYP2D7P, TCF20
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)nssv10327
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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