A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9646



Internal ID15193471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87928354..87976664hg38UCSC Ensembl
Outerchr4:88849506..88897816hg19UCSC Ensembl
Outerchr4:89068530..89116840hg18UCSC Ensembl
Outerchr4:89206685..89254995hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3848311
hg1948311
hg1848311
hg1748311
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7364
Supporting Variants
SamplesNA18507
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)nssv9646
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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