A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11066



Internal ID15192956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:107965612..108021480hg38UCSC Ensembl
Outerchr3:107684459..107740327hg19UCSC Ensembl
Outerchr3:109167149..109223017hg18UCSC Ensembl
Outerchr3:109167149..109223017hg17UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3855869
hg1955869
hg1855869
hg1755869
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7355
Supporting Variants
SamplesNA15510
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)nssv11066
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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