A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10669



Internal ID15195443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69099228..69135513hg38UCSC Ensembl
Outerchr9:71714144..71750429hg19UCSC Ensembl
Outerchr9:70903964..70940249hg18UCSC Ensembl
Outerchr9:68943698..68979983hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3836286
hg1936286
hg1836286
hg1736286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550
Supporting Variants
SamplesNA18956
Known GenesFXN, TJP2
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)nssv10669
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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