A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6738



Internal ID15551677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:131597831..131630705hg38UCSC Ensembl
Outerchr9:134473218..134506092hg19UCSC Ensembl
Outerchr9:133463039..133495913hg18UCSC Ensembl
Outerchr9:131502772..131535646hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg386406
hg196406
hg186406
hg176406
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5184
SamplesNA19129
Known GenesRAPGEF1
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)nsv6738
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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