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nsv5657953

  • 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: 219 SVs from 42 studies. See in: genome view    
Submitted genomic121,747,713-121,747,713Question Mark
Overlapping variant regions from other studies: 219 SVs from 42 studies. See in: genome view    
Remapped(Score: Perfect):122,185,619-122,185,619Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5657953Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr12121,747,713121,747,713
nsv5657953RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr12122,185,619122,185,619

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv17077625insertionSAMN00007882SequencingSequence alignment1,354

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17077625Submitted genomicNC_000012.12:g.121
747713_121747714in
s767
GRCh38 (hg38)NC_000012.12Chr12121,747,713121,747,713
nssv17077625RemappedPerfectNC_000012.11:g.122
185619_122185620in
s767
GRCh37.p13First PassNC_000012.11Chr12122,185,619122,185,619

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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