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esv1841832

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,765,645

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 7122 SVs from 127 studies. See in: genome view    
Remapped(Score: Pass):46,157,935-47,923,579Question Mark
Overlapping variant regions from other studies: 5258 SVs from 121 studies. See in: genome view    
Remapped(Score: Good):46,691,159-47,704,605Question Mark
Overlapping variant regions from other studies: 4158 SVs from 74 studies. See in: genome view    
Remapped(Score: Pass):431,049-2,010,264Question Mark
Overlapping variant regions from other studies: 2566 SVs from 36 studies. See in: genome view    
Submitted genomic46,111,165-47,174,611Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
esv1841832RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1046,157,93547,923,579
esv1841832RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1046,691,15947,704,605
esv1841832RemappedPassGRCh37.p13PATCHESFirst PassNW_003871068.1Chr10|NW_0
03871068.1
431,0492,010,264
esv1841832Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000010.9Chr1046,111,16547,174,611

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
essv4427906copy number gainNA10851SNP arraySNP genotyping analysis9,157

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
essv4427906RemappedPassNC_000010.11:g.(?_
46157935)_(4792357
9_?)dup
GRCh38.p12First PassNC_000010.11Chr1046,157,93547,923,579
essv4427906RemappedPassNW_003871068.1:g.(
?_431049)_(2010264
_?)dup
GRCh37.p13First PassNW_003871068.1Chr10|NW_0
03871068.1
431,0492,010,264
essv4427906RemappedGoodNC_000010.10:g.(?_
46691159)_(4770460
5_?)dup
GRCh37.p13First PassNC_000010.10Chr1046,691,15947,704,605
essv4427906Submitted genomicNC_000010.9:g.(?_4
6111165)_(47174611
_?)dup
NCBI36 (hg18)NC_000010.9Chr1046,111,16547,174,611

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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