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esv2760965

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:134,275

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 705 SVs from 74 studies. See in: genome view    
Remapped(Score: Perfect):238,486,457-238,620,731Question Mark
Overlapping variant regions from other studies: 710 SVs from 74 studies. See in: genome view    
Remapped(Score: Perfect):238,649,757-238,784,031Question Mark
Overlapping variant regions from other studies: 275 SVs from 23 studies. See in: genome view    
Submitted genomic236,716,380-236,850,654Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartOuter Stop
esv2760965RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr1238,486,457238,620,731
esv2760965RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1238,649,757238,784,031
esv2760965Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000001.9Chr1236,716,380236,850,654

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7005933copy number gainSW_1057SNP arraySNP genotyping analysis41
essv7005944copy number gainSW_1309SNP arraySNP genotyping analysis40

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7005933RemappedPerfectNC_000001.11:g.(?_
238486457)_(238620
731_?)dup
GRCh38.p12First PassNC_000001.11Chr1238,486,457238,620,731
essv7005944RemappedPerfectNC_000001.11:g.(?_
238491255)_(238615
306_?)dup
GRCh38.p12First PassNC_000001.11Chr1238,491,255238,615,306
essv7005933RemappedPerfectNC_000001.10:g.(?_
238649757)_(238784
031_?)dup
GRCh37.p13First PassNC_000001.10Chr1238,649,757238,784,031
essv7005944RemappedPerfectNC_000001.10:g.(?_
238654555)_(238778
606_?)dup
GRCh37.p13First PassNC_000001.10Chr1238,654,555238,778,606
essv7005933Submitted genomicNC_000001.9:g.(?_2
36716380)_(2368506
54_?)dup
NCBI36 (hg18)NC_000001.9Chr1236,716,380236,850,654
essv7005944Submitted genomicNC_000001.9:g.(?_2
36721178)_(2368452
29_?)dup
NCBI36 (hg18)NC_000001.9Chr1236,721,178236,845,229

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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