A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5169



Internal ID15542884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:90666126..90711064hg38UCSC Ensembl
Outerchr9:93428408..93473346hg19UCSC Ensembl
Outerchr9:92468228..92513166hg18UCSC Ensembl
Outerchr9:90507962..90552900hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3844939
hg1944939
hg1844939
hg1744939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610
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)nssv5169
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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