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nsv4377268

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:24,709

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 210 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):27,637,674-27,662,382Question Mark
Overlapping variant regions from other studies: 210 SVs from 49 studies. See in: genome view    
Submitted genomic27,926,603-27,951,311Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4377268RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1027,637,67427,662,382
nsv4377268Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000010.10Chr1027,926,60327,951,311

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15613771copy number loss1-0722-003SNP arrayGenotyping15

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15613771RemappedPerfectNC_000010.11:g.(?_
27637674)_(2766238
2_?)del
GRCh38.p12First PassNC_000010.11Chr1027,637,67427,662,382
nssv15613771Submitted genomicNC_000010.10:g.(?_
27926603)_(2795131
1_?)del
GRCh37 (hg19)NC_000010.10Chr1027,926,60327,951,311

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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