A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3580



Internal ID15201518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:24931195..24975258hg38UCSC Ensembl
Outerchr22:25327162..25371225hg19UCSC Ensembl
Outerchr22:23657162..23701225hg18UCSC Ensembl
Outerchr22:23651716..23695779hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3844064
hg1944064
hg1844064
hg1744064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4580
SamplesNA12878
Known GenesTMEM211
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)nsv3580
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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