A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6659



Internal ID15204904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:108856263..108890282hg38UCSC Ensembl
Outerchr9:111618543..111652562hg19UCSC Ensembl
Outerchr9:110658364..110692383hg18UCSC Ensembl
Outerchr9:108698098..108732117hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385724
hg195724
hg185724
hg175724
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739
SamplesNA12878
Known GenesACTL7A, IKBKAP
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)nsv6659
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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