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esv34111

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:288,106

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1258 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):24,781,123-25,069,228Question Mark
Overlapping variant regions from other studies: 1258 SVs from 81 studies. See in: genome view    
Remapped(Score: Perfect):24,802,669-25,090,774Question Mark
Overlapping variant regions from other studies: 442 SVs from 22 studies. See in: genome view    
Submitted genomic24,759,245-25,047,350Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv34111RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1124,781,12325,069,228
esv34111RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1124,802,66925,090,774
esv34111Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr1124,759,24525,047,350

Variant Call Information

Variant Call IDTypeMethodAnalysis
essv6990598copy number lossSNP arraySNP genotyping analysis

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv6990598RemappedPerfectNC_000011.10:g.(?_
24781123)_(2506922
8_?)del
GRCh38.p12First PassNC_000011.10Chr1124,781,12325,069,228
essv6990598RemappedPerfectNC_000011.9:g.(?_2
4802669)_(25090774
_?)del
GRCh37.p13First PassNC_000011.9Chr1124,802,66925,090,774
essv6990598Submitted genomicNC_000011.8:g.(?_2
4759245)_(25047350
_?)del
NCBI36 (hg18)NC_000011.8Chr1124,759,24525,047,350

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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