A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7224



Internal ID15205526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118564699..118571045hg38UCSC Ensembl
Outerchr11:118435414..118441760hg19UCSC Ensembl
Outerchr11:117940624..117946970hg18UCSC Ensembl
Outerchr11:117940624..117946970hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg386347
hg196347
hg186347
hg176347
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5384
SamplesNA19129
Known GenesIFT46
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)nsv7224
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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