A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5856



Internal ID15196850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:234137731..234187612hg18UCSC Ensembl
Outerchr2:234254992..234304873hg17UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg1849882
hg1749882
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7336
Supporting Variants
SamplesNA19129
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)nssv5856
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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