U.S. flag

An official website of the United States government

esv2527591

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:41,235

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2181 SVs from 87 studies. See in: genome view    
Remapped(Score: Perfect):32,475,759-32,516,993Question Mark
Overlapping variant regions from other studies: 2183 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):32,487,080-32,528,314Question Mark
Overlapping variant regions from other studies: 1568 SVs from 28 studies. See in: genome view    
Submitted genomic32,394,581-32,435,815Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2527591RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000016.10Chr1632,475,75932,516,993
esv2527591RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1632,487,08032,528,314
esv2527591Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000016.8Chr1632,394,58132,435,815

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv5281870copy number gainNA18507SequencingRead depth232,775

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv5281870RemappedPerfectNC_000016.10:g.(?_
32475759)_(3251699
3_?)dup
GRCh38.p12First PassNC_000016.10Chr1632,475,75932,516,993
essv5281870RemappedPerfectNC_000016.9:g.(?_3
2487080)_(32528314
_?)dup
GRCh37.p13First PassNC_000016.9Chr1632,487,08032,528,314
essv5281870Submitted genomicNC_000016.8:g.(?_3
2394581)_(32435815
_?)dup
NCBI36 (hg18)NC_000016.8Chr1632,394,58132,435,815

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

Support Center