A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9399



Internal ID15193664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87928476..87976378hg38UCSC Ensembl
Outerchr4:88849628..88897530hg19UCSC Ensembl
Outerchr4:89068652..89116554hg18UCSC Ensembl
Outerchr4:89206807..89254709hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3847903
hg1947903
hg1847903
hg1747903
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA18517
Known GenesSPP1
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)nssv9399
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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