A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5175



Internal ID15196148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:113079872..113112432hg38UCSC Ensembl
Outerchr9:115842152..115874712hg19UCSC Ensembl
Outerchr9:114881973..114914533hg18UCSC Ensembl
Outerchr9:112921706..112954266hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3832561
hg1932561
hg1832561
hg1732561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7431
Supporting Variants
SamplesNA19129
Known GenesFAM225B
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)nssv5175
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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