esv5440

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,977

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 121 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):157,203,831-157,205,807Question Mark
Overlapping variant regions from other studies: 118 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):157,173,621-157,175,597Question Mark
Overlapping variant regions from other studies: 101 SVs from 15 studies. See in: genome view    
Submitted genomic155,440,245-155,442,221Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
esv5440RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr1157,203,831157,204,054157,205,605157,205,807
esv5440RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr1157,173,621157,173,844157,175,395157,175,597
esv5440Submitted genomicNCBI36 (hg18)NC_000001.9Chr1155,440,245155,440,468155,442,019155,442,221

Variant Call Information

Variant Call IDTypeMethodAnalysis
essv27881copy number lossSequencingRead depth and paired-end mapping

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
essv27881RemappedPerfectNC_000001.11:g.(15
7203831_157204054)
_(157205605_157205
807)del
GRCh38 (hg38)Primary AssemblyFirst PassNC_000001.11Chr1157,203,831157,204,054157,205,605157,205,807
essv27881RemappedPerfectNC_000001.10:g.(15
7173621_157173844)
_(157175395_157175
597)del
GRCh37 (hg19)Primary AssemblyFirst PassNC_000001.10Chr1157,173,621157,173,844157,175,395157,175,597
essv27881Submitted genomicNC_000001.9:g.(155
440245_155440468)_
(155442019_1554422
21)del
NCBI36 (hg18)NC_000001.9Chr1155,440,245155,440,468155,442,019155,442,221

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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