A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6641



Internal ID15204885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:101343597..101365101hg38UCSC Ensembl
Outerchr9:104105879..104127383hg19UCSC Ensembl
Outerchr9:103145700..103167204hg18UCSC Ensembl
Outerchr9:101185434..101206938hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg389154
hg199154
hg189154
hg179154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5172
SamplesNA19129
Known GenesBAAT
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)nsv6641
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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