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esv4002935

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):8,041,660-8,041,660Question Mark
Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):135,561,236-135,561,236Question Mark
Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
Submitted genomic8,181,790-8,181,790Question Mark
Overlapping variant regions from other studies: 131 SVs from 25 studies. See in: genome view    
Submitted genomic135,245,984-135,245,984Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStopstrand
esv4002935RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr28,041,6608,041,660+
esv4002935RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000007.14Chr7135,561,236135,561,236+
esv4002935Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000002.11Chr28,181,7908,181,790+
esv4002935Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000007.13Chr7135,245,984135,245,984+

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv26058942interchromosomal translocation10001047_1_1SequencingSplit read and paired-end mappingessv26058945, essv26058944, essv26058943

Variant Call Placement Information

Variant Call IDPlacement TypeScoreAssemblyReciprocitySequence IDChrStartStopstrand
essv26058942RemappedPerfectGRCh38.p12First PassNC_000002.12Chr28,041,6608,041,660+
essv26058942RemappedPerfectGRCh38.p12First PassNC_000007.14Chr7135,561,236135,561,236+
essv26058942Submitted genomicGRCh37 (hg19)NC_000002.11Chr28,181,7908,181,790+
essv26058942Submitted genomicGRCh37 (hg19)NC_000007.13Chr7135,245,984135,245,984+

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
essv26058942210001047_1_1SequencingSequence alignmentPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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