A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10672



Internal ID15542126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:70692709..70744744hg38UCSC Ensembl
Outerchr9:73307625..73359660hg19UCSC Ensembl
Outerchr9:72497445..72549480hg18UCSC Ensembl
Outerchr9:70537179..70589214hg17UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3852036
hg1952036
hg1852036
hg1752036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6556
Supporting Variants
SamplesNA18956
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)nssv10672
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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