A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1916



Internal ID15194513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:274834..316239hg38UCSC Ensembl
Outerchr11:274834..316239hg19UCSC Ensembl
Outerchr11:264834..306239hg18UCSC Ensembl
Outerchr11:264834..306239hg17UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3841406
hg1941406
hg1841406
hg1741406
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7212
Supporting Variants
SamplesNA18555
Known GenesATHL1, IFITM1, 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)nssv1916
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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