A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5152



Internal ID15542933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:17836355..17864940hg38UCSC Ensembl
Outerchr9:17836353..17864938hg19UCSC Ensembl
Outerchr9:17826353..17854938hg18UCSC Ensembl
Outerchr9:17826353..17854938hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3810694
hg1910694
hg1810694
hg1710694
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6492
Supporting Variants
SamplesNA19129
Known Genes
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)nssv5152
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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