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esv2513311

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,509

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 428 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):132,237,596-132,246,104Question Mark
Overlapping variant regions from other studies: 428 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):132,995,169-133,003,677Question Mark
Overlapping variant regions from other studies: 200 SVs from 21 studies. See in: genome view    
Submitted genomic132,711,639-132,720,147Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2513311RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2132,237,596132,246,104
esv2513311RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,995,169133,003,677
esv2513311Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000002.10Chr2132,711,639132,720,147

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5212883copy number gainNA18507SequencingRead depth232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5212883RemappedPerfectNC_000002.12:g.(?_
132237596)_(132246
104_?)dup
GRCh38.p12First PassNC_000002.12Chr2132,237,596132,246,104
essv5212883RemappedPerfectNC_000002.11:g.(?_
132995169)_(133003
677_?)dup
GRCh37.p13First PassNC_000002.11Chr2132,995,169133,003,677
essv5212883Submitted genomicNC_000002.10:g.(?_
132711639)_(132720
147_?)dup
NCBI36 (hg18)NC_000002.10Chr2132,711,639132,720,147

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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