A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471677



Internal ID15214496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:103635373..103750710hg38UCSC Ensembl
Innerchr1:104177995..104293332hg19UCSC Ensembl
Innerchr1:103979518..104094855hg18UCSC Ensembl
Innerchr1:103532648..103647985hg16UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38115338
hg19115338
hg18115338
hg16115338
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv548766, nssv548735, nssv548756, nssv548761, nssv548765, nssv548734, nssv548736, nssv548769, nssv548755, nssv548753, nssv548752, nssv548742, nssv548741, nssv548731, nssv548771, nssv548745, nssv548749, nssv548748, nssv548763, nssv548751, nssv548730, nssv548747, nssv548739, nssv548767, nssv548754, nssv548746, nssv548750, nssv548757, nssv548740, nssv548728, nssv548768, nssv548744, nssv548762, nssv548758, nssv548732, nssv548729, nssv548733, nssv548727, nssv548770, nssv548760, nssv548764, nssv548759, nssv548738
SamplesNA10971, NA15732, JK1051A, NA10469, JK776, P86GA, NA16689, NA17059, NA17058, NA10473, NA10496, NA17015, NA10492, NA15728, NA15725, NA15733, NA11521, NA15731, NA10470, NA17052, NA10979, NA11523, NA10969, NA10471, NA10472, NA15724, JK1688B, NA17016, NA11776, NA10967, JK1058B, NA10976, JK1061, NA10495, NA10494, NA17017, NA17051, NA15729, NA17014, NA15730, NA16688, NA10493, NA10970
Known GenesAMY1A, AMY1B, AMY1C
MethodBAC aCGH
AnalysisArray image analysis and normalization were performed using UCSF Spot and Sproc software (Jain et al. 2002). BACs for which only one of the triplicates printed on the array yielded data, or for which the standard deviation of log2 ratio for the triplicates was 10.2, were removed from final analysis. Furthermore, we discarded BACs that failed to yield data in <20% of cases. For each hybridization experiment, we established a threshold log2 ratio of 2 SDs from the mean of all autosomal clones, and BACs that exceeded this threshold in both independent dye-swap experiments were classified as variant.
PlatformGPL4010
Comments
ReferenceSharp_et_al_2005
Pubmed ID15918152
Accession Number(s)nsv471677
Frequency
Sample Size48
Observed Gain1
Observed Loss42
Observed Complex0
Frequencyn/a


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