A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7219



Internal ID15205520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:62058808..62141019hg38UCSC Ensembl
Outerchr11:61826280..61908491hg19UCSC Ensembl
Outerchr11:61582856..61665067hg18UCSC Ensembl
Outerchr11:61582856..61665067hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3882212
hg1982212
hg1882212
hg1782212
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1941, nssv9271
SamplesNA18555, NA18517
Known GenesINCENP
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)nsv7219
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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