A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7205



Internal ID8519173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77992865..78011647hg38UCSC Ensembl
Outerchr10:79752623..79771405hg19UCSC Ensembl
Outerchr10:79422629..79441411hg18UCSC Ensembl
Outerchr10:79422629..79441411hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3818783
hg1918783
hg1818783
hg1718783
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv951
SamplesNA19240
Known GenesPOLR3A
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)nsv7205
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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