A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6745



Internal ID15204999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132929207..132958453hg38UCSC Ensembl
Outerchr9:135804594..135833840hg19UCSC Ensembl
Outerchr9:134794415..134823661hg18UCSC Ensembl
Outerchr9:132834148..132863394hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3810987
hg1910987
hg1810987
hg1710987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9924, nssv6298
SamplesNA18507, NA12156
Known GenesTSC1
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)nsv6745
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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