A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7364



Internal ID15205680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87888542..87976664hg38UCSC Ensembl
Outerchr4:88809694..88897816hg19UCSC Ensembl
Outerchr4:89028718..89116840hg18UCSC Ensembl
Outerchr4:89166873..89254995hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3888123
hg1988123
hg1888123
hg1788123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7101, nssv9645, nssv10411, nssv398, nssv9399, nssv4762, nssv3269, nssv11088, nssv7102, nssv4763, nssv9646
SamplesNA18507, NA12156, NA12878, NA18956, NA15510, NA18517, NA19240, NA19129
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)nsv7364
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer