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nsv2729032

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,617,019

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 6437 SVs from 104 studies. See in: genome view    
Remapped(Score: Pass):34,370,225-37,987,243Question Mark
Overlapping variant regions from other studies: 5400 SVs from 103 studies. See in: genome view    
Remapped(Score: Pass):34,523,160-38,381,045Question Mark
Overlapping variant regions from other studies: 1770 SVs from 31 studies. See in: genome view    
Submitted genomic34,414,427-36,667,312Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv2729032RemappedPassGRCh38.p12Primary AssemblyFirst PassNC_000012.12Chr1234,370,22537,987,243
nsv2729032RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1234,523,16038,381,045
nsv2729032Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000012.10Chr1234,414,42736,667,312

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv13588684deletionSNP arrayProbe signal intensity

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv13588684RemappedPassNC_000012.12:g.(?_
34370225)_(3798724
3_?)del
GRCh38.p12First PassNC_000012.12Chr1234,370,22537,987,243
nssv13588684RemappedPassNC_000012.11:g.(?_
34523160)_(3838104
5_?)del
GRCh37.p13First PassNC_000012.11Chr1234,523,16038,381,045
nssv13588684Submitted genomicNC_000012.10:g.(?_
34414427)_(3666731
2_?)del
NCBI36 (hg18)NC_000012.10Chr1234,414,42736,667,312

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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