A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3648



Internal ID15548278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:44417435..44462167hg38UCSC Ensembl
Outerchr22:44813315..44858047hg19UCSC Ensembl
Outerchr22:43191979..43236711hg18UCSC Ensembl
Outerchr22:43133852..43178584hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3844733
hg1944733
hg1844733
hg1744733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7753
SamplesNA12156
Known Genes
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)nsv3648
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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