esv2425290

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 27 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):20,400,841-20,400,843Question Mark
Overlapping variant regions from other studies: 28 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):20,401,072-20,401,074Question Mark
Overlapping variant regions from other studies: 25 SVs from 6 studies. See in: genome view    
Submitted genomic20,509,051-20,509,053Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
esv2425290RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr620,400,84120,400,843
esv2425290RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000006.11Chr620,401,07220,401,074
esv2425290Submitted genomicNCBI36 (hg18)NC_000006.10Chr620,509,05120,509,053

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5175894deletionNA18507SequencingSplit read mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrStartStop
essv5175894RemappedPerfectNC_000006.12:g.20400841_20400843delGRCh38 (hg38)Primary AssemblyFirst PassNC_000006.12Chr620,400,84120,400,843
essv5175894RemappedPerfectNC_000006.11:g.20401072_20401074delGRCh37 (hg19)Primary AssemblyFirst PassNC_000006.11Chr620,401,07220,401,074
essv5175894Submitted genomicNC_000006.10:g.20509051_20509053delNCBI36 (hg18)NC_000006.10Chr620,509,05120,509,053

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant