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esv1847684

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:267,140

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 998 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):53,611,841-53,878,980Question Mark
Overlapping variant regions from other studies: 1003 SVs from 75 studies. See in: genome view    
Remapped(Score: Perfect):55,371,601-55,638,740Question Mark
Overlapping variant regions from other studies: 367 SVs from 24 studies. See in: genome view    
Submitted genomic55,041,607-55,308,746Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv1847684RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1053,611,84153,878,980
esv1847684RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1055,371,60155,638,740
esv1847684Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr1055,041,60755,308,746

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv4396500copy number lossNA18980SNP arraySNP genotyping analysis9,229

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv4396500RemappedPerfectNC_000010.11:g.(?_
53611841)_(5387898
0_?)del
GRCh38.p12First PassNC_000010.11Chr1053,611,84153,878,980
essv4396500RemappedPerfectNC_000010.10:g.(?_
55371601)_(5563874
0_?)del
GRCh37.p13First PassNC_000010.10Chr1055,371,60155,638,740
essv4396500Submitted genomicNC_000010.9:g.(?_5
5041607)_(55308746
_?)del
NCBI36 (hg18)NC_000010.9Chr1055,041,60755,308,746

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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