A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv841



Internal ID15198113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133306977..133317987hg38UCSC Ensembl
Outerchr9:136182373..136184822hg19UCSC Ensembl
Outerchr9:135172194..135174643hg18UCSC Ensembl
Outerchr9:133211927..133214376hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg389249
hg199249
hg189249
hg179249
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6749
Supporting Variants
SamplesNA19240
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)nssv841
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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