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esv1914954

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:707,446

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3385 SVs from 100 studies. See in: genome view    
Remapped(Score: Perfect):5,997,691-6,705,136Question Mark
Overlapping variant regions from other studies: 3385 SVs from 100 studies. See in: genome view    
Remapped(Score: Perfect):6,037,322-6,744,767Question Mark
Overlapping variant regions from other studies: 112 SVs from 11 studies. See in: genome view    
Submitted genomic5,810,563-6,518,007Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv1914954RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr75,997,6916,705,136
esv1914954RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr76,037,3226,744,767
esv1914954Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000007.11Chr75,810,5636,518,007

Variant Call Information

Variant Call IDTypeMethodAnalysis
essv4491061inversionFISHManual observation

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv4491061RemappedPerfectNC_000007.14:g.(59
97691_?)_(?_670513
6)inv
GRCh38.p12First PassNC_000007.14Chr75,997,6916,705,136
essv4491061RemappedPerfectNC_000007.13:g.(60
37322_?)_(?_674476
7)inv
GRCh37.p13First PassNC_000007.13Chr76,037,3226,744,767
essv4491061Submitted genomicNC_000007.11:g.(58
10563_?)_(?_651800
7)inv
NCBI35 (hg17)NC_000007.11Chr75,810,5636,518,007

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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