A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9924



Internal ID15193323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132930794..132958453hg38UCSC Ensembl
Outerchr9:135806181..135833840hg19UCSC Ensembl
Outerchr9:134796002..134823661hg18UCSC Ensembl
Outerchr9:132835735..132863394hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385966
hg195966
hg185966
hg175966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6745
Supporting Variants
SamplesNA18507
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)nssv9924
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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