A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517314



Internal ID15097921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:15531057..15554099hg38UCSC Ensembl
Innerchr8:15388566..15411608hg19UCSC Ensembl
Innerchr8:15432937..15455979hg18UCSC Ensembl
Innerchr8:15432937..15455979hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3823043
hg1923043
hg1823043
hg1723043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671202, nssv653316, nssv674943, nssv661813, nssv679013, nssv654365, nssv691087, nssv676455, nssv686628, nssv654911, nssv685080, nssv664601, nssv671601, nssv669105, nssv681491, nssv669461, nssv679454, nssv678765, nssv660097, nssv670298, nssv663407, nssv678110, nssv659063, nssv678262, nssv659565, nssv689988, nssv685623, nssv673287, nssv661853, nssv674798, nssv692160, nssv690557, nssv682735, nssv652298, nssv688195, nssv671383, nssv673765, nssv676364, nssv658534, nssv657645, nssv655723, nssv680236, nssv665655, nssv689654, nssv666981, nssv652358, nssv661773, nssv677464, nssv676065, nssv656624, nssv688143, nssv669614, nssv680662, nssv687251, nssv663978, nssv678178, nssv691147, nssv682665, nssv693770, nssv675588, nssv677860, nssv674013, nssv669914, nssv660462, nssv672360, nssv684342, nssv684877, nssv683010, nssv651686, nssv658113, nssv667905, nssv681726, nssv656955, nssv693045, nssv656081, nssv672940
Samples
Known GenesTUSC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517314
Frequency
Sample Size2026
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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