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esv2460496

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13,295

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 415 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):110,833,463-110,846,757Question Mark
Overlapping variant regions from other studies: 417 SVs from 71 studies. See in: genome view    
Remapped(Score: Perfect):111,376,085-111,389,379Question Mark
Overlapping variant regions from other studies: 196 SVs from 25 studies. See in: genome view    
Submitted genomic111,177,608-111,190,902Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
esv2460496RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1110,833,463110,846,757
esv2460496RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1111,376,085111,389,379
esv2460496Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1111,177,608111,190,902

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5254911deletionNA18507SequencingPaired-end mapping232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
essv5254911RemappedPerfectNC_000001.11:g.(11
0833463_?)_(?_1108
46757)del
GRCh38.p12First PassNC_000001.11Chr1110,833,463110,846,757
essv5254911RemappedPerfectNC_000001.10:g.(11
1376085_?)_(?_1113
89379)del
GRCh37.p13First PassNC_000001.10Chr1111,376,085111,389,379
essv5254911Submitted genomicNC_000001.9:g.(111
177608_?)_(?_11119
0902)del
NCBI36 (hg18)NC_000001.9Chr1111,177,608111,190,902

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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