A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5332



Internal ID15196603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:274261..313815hg38UCSC Ensembl
Outerchr11:274261..313815hg19UCSC Ensembl
Outerchr11:264261..303815hg18UCSC Ensembl
Outerchr11:264261..303815hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3839555
hg1939555
hg1839555
hg1739555
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7212
Supporting Variants
SamplesNA19129
Known GenesATHL1, IFITM2, IFITM5, NLRP6
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)nssv5332
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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