Variant DetailsVariant: nsv7278Internal ID | 15205585 | Landmark | | Location Information | | Cytoband | 16p12.3 | Allele length | Assembly | Allele length | hg38 | 2140982 | hg19 | 2058447 | hg18 | 2058447 | hg17 | 2058447 |
| Variant Type | OTHER inversion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv2135, nssv10084 | Samples | NA18956, NA18555 | Known Genes | ABCC6P1, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR6511A-2, MIR6770-2, NOMO2, NPIPA7, NPIPA8, XYLT1 | Method | Sequencing | Analysis | End-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005) | Platform | Capillary | Comments | | Reference | Kidd_et_al_2008 | Pubmed ID | 18451855 | Accession Number(s) | nsv7278
| Frequency | Sample Size | 9 | Observed Gain | 0 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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