A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6280



Internal ID15537583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70701381..70739076hg38UCSC Ensembl
Outerchr9:73316297..73353992hg19UCSC Ensembl
Outerchr9:72506117..72543812hg18UCSC Ensembl
Outerchr9:70545851..70583546hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3837696
hg1937696
hg1837696
hg1737696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556
Supporting Variants
SamplesNA12156
Known GenesTRPM3
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)nssv6280
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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