A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10674



Internal ID15542124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:87911997..87915919hg38UCSC Ensembl
Outerchr9:90526912..90530834hg19UCSC Ensembl
Outerchr9:89716732..89720654hg18UCSC Ensembl
Outerchr9:87756466..87760388hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg387337
hg197337
hg187337
hg177337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6599
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)nssv10674
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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