A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5333



Internal ID15196601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:313228..355146hg38UCSC Ensembl
Outerchr11:313228..355146hg19UCSC Ensembl
Outerchr11:303228..345146hg18UCSC Ensembl
Outerchr11:303228..345146hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3841919
hg1941919
hg1841919
hg1741919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7212
Supporting Variants
SamplesNA19129
Known GenesIFITM1, IFITM3
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)nssv5333
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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