U.S. flag

An official website of the United States government

esv2830317

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:35,623

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 380 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):165,324,003-165,359,625Question Mark
Overlapping variant regions from other studies: 380 SVs from 67 studies. See in: genome view    
Remapped(Score: Perfect):165,041,791-165,077,413Question Mark
Overlapping variant regions from other studies: 129 SVs from 23 studies. See in: genome view    
Submitted genomic166,524,485-166,560,107Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2830317RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3165,324,003165,359,625
esv2830317RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3165,041,791165,077,413
esv2830317Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000003.10Chr3166,524,485166,560,107

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeCopy number
essv7099022copy number lossSNP arrayProbe signal intensityRecurrent miscarriage1
essv7099023copy number lossSNP arrayProbe signal intensityRecurrent miscarriage1

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7099022RemappedPerfectNC_000003.12:g.(?_
165324003)_(165359
625_?)del
GRCh38.p12First PassNC_000003.12Chr3165,324,003165,359,625
essv7099023RemappedPerfectNC_000003.12:g.(?_
165324003)_(165359
625_?)del
GRCh38.p12First PassNC_000003.12Chr3165,324,003165,359,625
essv7099022RemappedPerfectNC_000003.11:g.(?_
165041791)_(165077
413_?)del
GRCh37.p13First PassNC_000003.11Chr3165,041,791165,077,413
essv7099023RemappedPerfectNC_000003.11:g.(?_
165041791)_(165077
413_?)del
GRCh37.p13First PassNC_000003.11Chr3165,041,791165,077,413
essv7099022Submitted genomicNC_000003.10:g.(?_
166524485)_(166560
107_?)del
NCBI36 (hg18)NC_000003.10Chr3166,524,485166,560,107
essv7099023Submitted genomicNC_000003.10:g.(?_
166524485)_(166560
107_?)del
NCBI36 (hg18)NC_000003.10Chr3166,524,485166,560,107

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