A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5159



Internal ID15196228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:69120707..69142577hg38UCSC Ensembl
Outerchr9:71735623..71757493hg19UCSC Ensembl
Outerchr9:70925443..70947313hg18UCSC Ensembl
Outerchr9:68965177..68987047hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3821871
hg1921871
hg1821871
hg1721871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6550
Supporting Variants
SamplesNA19129
Known GenesTJP2
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)nssv5159
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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