A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517465



Internal ID15444758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:89701126..89725784hg38UCSC Ensembl
Innerchr14:90167470..90192128hg19UCSC Ensembl
Innerchr14:89237223..89261881hg18UCSC Ensembl
Innerchr14:89237223..89261881hg17UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg3824659
hg1924659
hg1824659
hg1724659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683918, nssv677297, nssv692092, nssv692402, nssv671260, nssv677447, nssv657761, nssv687290, nssv679168, nssv693057, nssv681156, nssv692846, nssv652093, nssv679295, nssv676257, nssv668629, nssv669998, nssv661101, nssv652427, nssv669901, nssv681689, nssv670344, nssv669503, nssv661672, nssv678120, nssv693850, nssv685905
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517465
Frequency
Sample Size2026
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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