A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9392



Internal ID15540343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:49260358..49313455hg38UCSC Ensembl
Outerchr4:49262375..49315472hg19UCSC Ensembl
Outerchr4:48957132..49010229hg18UCSC Ensembl
Outerchr4:49103303..49156400hg17UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3853098
hg1953098
hg1853098
hg1753098
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7360
Supporting Variants
SamplesNA18517
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)nssv9392
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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