A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9474



Internal ID15193502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123939138..123990437hg38UCSC Ensembl
Outerchr9:126701417..126752716hg19UCSC Ensembl
Outerchr9:125741238..125792537hg18UCSC Ensembl
Outerchr9:123780971..123832270hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3851300
hg1951300
hg1851300
hg1751300
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7435
Supporting Variants
SamplesNA18517
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)nssv9474
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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