A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7353



Internal ID15552354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:50846253..50937800hg38UCSC Ensembl
Outerchr3:50883684..50975231hg19UCSC Ensembl
Outerchr3:50858688..50950271hg18UCSC Ensembl
Outerchr3:50858688..50950271hg17UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3891548
hg1991548
hg1891584
hg1791584
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10343, nssv3163, nssv3164, nssv5966, nssv11058, nssv5967, nssv11059, nssv9618, nssv9381, nssv10342, nssv300, nssv2395
SamplesNA18507, NA12878, NA18956, NA15510, NA18555, NA18517, NA19240, NA19129
Known GenesDOCK3
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)nsv7353
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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