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esv2763423

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:46,187

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 536 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):184,642,465-184,688,651Question Mark
Overlapping variant regions from other studies: 536 SVs from 62 studies. See in: genome view    
Remapped(Score: Perfect):185,563,619-185,609,805Question Mark
Overlapping variant regions from other studies: 241 SVs from 16 studies. See in: genome view    
Submitted genomic185,800,613-185,846,799Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv2763423RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000004.12Chr4184,642,465184,688,651
esv2763423RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4185,563,619185,609,805
esv2763423Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000004.10Chr4185,800,613185,846,799

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv7030380copy number lossSW_0379SNP arraySNP genotyping analysis43

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv7030380RemappedPerfectNC_000004.12:g.(?_
184642465)_(184688
651_?)del
GRCh38.p12First PassNC_000004.12Chr4184,642,465184,688,651
essv7030380RemappedPerfectNC_000004.11:g.(?_
185563619)_(185609
805_?)del
GRCh37.p13First PassNC_000004.11Chr4185,563,619185,609,805
essv7030380Submitted genomicNC_000004.10:g.(?_
185800613)_(185846
799_?)del
NCBI36 (hg18)NC_000004.10Chr4185,800,613185,846,799

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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