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esv2607576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:11,388

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 463 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):193,156,957-193,168,344Question Mark
Overlapping variant regions from other studies: 463 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):192,874,746-192,886,133Question Mark
Overlapping variant regions from other studies: 264 SVs from 29 studies. See in: genome view    
Submitted genomic194,357,440-194,368,827Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2607576RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3193,156,957193,168,344
esv2607576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3192,874,746192,886,133
esv2607576Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr3194,357,440194,368,827

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5239695deletionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5239695RemappedPerfectNC_000003.12:g.(19
3156957_?)_(?_1931
68344)del
GRCh38.p12First PassNC_000003.12Chr3193,156,957193,168,344
essv5239695RemappedPerfectNC_000003.11:g.(19
2874746_?)_(?_1928
86133)del
GRCh37.p13First PassNC_000003.11Chr3192,874,746192,886,133
essv5239695Submitted genomicNC_000003.10:g.(19
4357440_?)_(?_1943
68827)del
NCBI36 (hg18)NC_000003.10Chr3194,357,440194,368,827

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

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