A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7366



Internal ID15205682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:170395212..170693088hg38UCSC Ensembl
Outerchr4:171316363..171614239hg19UCSC Ensembl
Outerchr4:171552938..171850814hg18UCSC Ensembl
Outerchr4:171691093..171988969hg17UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38297877
hg19297877
hg18297877
hg17297877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3304
SamplesNA12878
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)nsv7366
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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