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nsv1163545

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 379 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):8,645,764-8,645,764Question Mark
Overlapping variant regions from other studies: 383 SVs from 32 studies. See in: genome view    
Submitted genomic8,645,764-8,645,764Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv1163545RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr98,645,7648,645,764
nsv1163545Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000009.11Chr98,645,7648,645,764

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv4042633alu insertionSequencingde novo and local sequence assembly

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv4042633RemappedPerfectNC_000009.12:g.864
5764_8645765ins289
GRCh38.p12First PassNC_000009.12Chr98,645,7648,645,764
nssv4042633Submitted genomicNC_000009.11:g.864
5764_8645765ins289
GRCh37 (hg19)NC_000009.11Chr98,645,7648,645,764

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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