A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3976



Internal ID15538703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:89935213..89947581hg38UCSC Ensembl
Outerchr11:89668381..89680749hg19UCSC Ensembl
Outerchr11:89308029..89320397hg18UCSC Ensembl
Outerchr11:89308029..89320397hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3812369
hg1912369
hg1812369
hg1712369
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7222
Supporting Variants
SamplesNA12878
Known GenesMIR5692A1
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)nssv3976
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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