A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6298



Internal ID15190880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:132929207..132957657hg38UCSC Ensembl
Outerchr9:135804594..135833044hg19UCSC Ensembl
Outerchr9:134794415..134822865hg18UCSC Ensembl
Outerchr9:132834148..132862598hg17UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3810987
hg1910987
hg1810987
hg1710987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6745
Supporting Variants
SamplesNA12156
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)nssv6298
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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