nsv819722

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:269

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 126 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):33,250,154-33,250,422Question Mark
Overlapping variant regions from other studies: 126 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):33,741,060-33,741,328Question Mark
Overlapping variant regions from other studies: 47 SVs from 14 studies. See in: genome view    
Submitted genomic38,432,900-38,433,168Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv819722RemappedPerfectGRCh38 (hg38)Primary AssemblyFirst PassNC_000019.10Chr1933,250,15433,250,422
nsv819722RemappedPerfectGRCh37 (hg19)Primary AssemblyFirst PassNC_000019.9Chr1933,741,06033,741,328
nsv819722Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000019.8Chr1938,432,90038,433,168

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1418901insertionSAMN00002681SequencingPaired-end mapping1,318

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv1418901RemappedPerfectNC_000019.10:g.(33
250154_?)_(?_33250
422)ins1064
GRCh38 (hg38)First PassNC_000019.10Chr1933,250,15433,250,422
nssv1418901RemappedPerfectNC_000019.9:g.(337
41060_?)_(?_337413
28)ins1064
GRCh37 (hg19)First PassNC_000019.9Chr1933,741,06033,741,328
nssv1418901Submitted genomicNC_000019.8:g.(384
32900_?)_(?_384331
68)ins1064
NCBI36 (hg18)NC_000019.8Chr1938,432,90038,433,168

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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