A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3589



Internal ID15201527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:28869176..28892947hg38UCSC Ensembl
Outerchr22:29265164..29288935hg19UCSC Ensembl
Outerchr22:27595164..27618935hg18UCSC Ensembl
Outerchr22:27589718..27613489hg17UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3823772
hg1923772
hg1823772
hg1723772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7737
SamplesNA12156
Known GenesZNRF3
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)nsv3589
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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