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nsv436883

  • Variant Calls:1
  • Validation:Yes
  • Clinical Assertions: No
  • Region Size:14,597

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 385 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):21,480,066-21,494,662Question Mark
Overlapping variant regions from other studies: 385 SVs from 63 studies. See in: genome view    
Remapped(Score: Perfect):21,480,175-21,494,771Question Mark
Overlapping variant regions from other studies: 146 SVs from 17 studies. See in: genome view    
Submitted genomic21,515,932-21,530,528Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv436883RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr521,480,06621,494,662
nsv436883RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr521,480,17521,494,771
nsv436883Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000005.8Chr521,515,93221,530,528

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv466204insertionSAMN00001583SequencingPaired-end mapping822

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv466204RemappedPerfectNC_000005.10:g.(21
480066_?)_(?_21494
662)ins?
GRCh38.p12First PassNC_000005.10Chr521,480,06621,494,662
nssv466204RemappedPerfectNC_000005.9:g.(214
80175_?)_(?_214947
71)ins?
GRCh37.p13First PassNC_000005.9Chr521,480,17521,494,771
nssv466204Submitted genomicNC_000005.8:g.(215
15932_?)_(?_215305
28)ins(0_?)
NCBI36 (hg18)NC_000005.8Chr521,515,93221,530,528

Validation Information

Variant Call IDExperiment IDSample IDMethodAnalysisResult
nssv4662044SAMN00001583PCRManual observationPass

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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