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esv992038

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:19,355

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 215 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):233,561,640-233,580,994Question Mark
Overlapping variant regions from other studies: 214 SVs from 42 studies. See in: genome view    
Remapped(Score: Pass):234,469,866-234,487,574Question Mark
Overlapping variant regions from other studies: 93 SVs from 16 studies. See in: genome view    
Submitted genomic234,135,025-234,154,379Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartOuter Stop
esv992038RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2233,561,640-233,580,994
esv992038RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2-234,469,866234,487,574
esv992038Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000002.10Chr2234,135,025-234,154,379

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv3565204inversionHuRefSequencingPaired-end mapping23,887

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartOuter Stop
essv3565204RemappedPerfectNC_000002.12:g.(23
3561640_?)_(?_2335
80994)inv19355
GRCh38.p12First PassNC_000002.12Chr2233,561,640-233,580,994
essv3565204RemappedPassNC_000002.11:g.(?_
234469866)_(?_2344
87574)inv19355
GRCh37.p13First PassNC_000002.11Chr2-234,469,866234,487,574
essv3565204Submitted genomicNC_000002.10:g.(23
4135025_?)_(?_2341
54379)inv19355
NCBI36 (hg18)NC_000002.10Chr2234,135,025-234,154,379

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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