A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11067



Internal ID15192955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:108007470..108056389hg38UCSC Ensembl
Outerchr3:107726317..107775236hg19UCSC Ensembl
Outerchr3:109209007..109257926hg18UCSC Ensembl
Outerchr3:109209007..109257926hg17UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3848920
hg1948920
hg1848920
hg1748920
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7355
Supporting Variants
SamplesNA15510
Known GenesCD47
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)nssv11067
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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