A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9589



Internal ID15193039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:233577887..233618408hg38UCSC Ensembl
Outerchr2:234486533..234527054hg19UCSC Ensembl
Outerchr2:234137851..234191793hg18UCSC Ensembl
Outerchr2:234255112..234309054hg17UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3840522
hg1940522
hg1853943
hg1753943
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7336
Supporting Variants
SamplesNA18507
Known GenesUGT1A8
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)nssv9589
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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