A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10690



Internal ID15195422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:133303882..133321861hg38UCSC Ensembl
Outerchr9:136179364..136188697hg19UCSC Ensembl
Outerchr9:135169185..135178518hg18UCSC Ensembl
Outerchr9:133208918..133218251hg17UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg389130
hg199130
hg189130
hg179130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6749
Supporting Variants
SamplesNA18956
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)nssv10690
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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