A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6746



Internal ID15205000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133044293..133068877hg38UCSC Ensembl
Outerchr9:135919680..135944264hg19UCSC Ensembl
Outerchr9:134909501..134934085hg18UCSC Ensembl
Outerchr9:132949234..132973818hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3815418
hg1915418
hg1815418
hg1715418
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1807, nssv10688
SamplesNA18956, NA18555
Known GenesCEL, GTF3C5, MIR6877
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)nsv6746
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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