A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7759



Internal ID15189419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:50391793..50436883hg38UCSC Ensembl
Outerchr22:50830222..50875312hg19UCSC Ensembl
Outerchr22:49177088..49222178hg18UCSC Ensembl
Outerchr22:49120366..49165456hg17UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg3845091
hg1945091
hg1845091
hg1745091
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3668
Supporting Variants
SamplesNA12156
Known GenesPPP6R2
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)nssv7759
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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