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nsv5963790

  • 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: 111 SVs from 27 studies. See in: genome view    
Submitted genomic109,217,059-109,217,059Question Mark
Overlapping variant regions from other studies: 111 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):110,138,215-110,138,215Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5963790Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4109,217,059109,217,059
nsv5963790RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4110,138,215110,138,215

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17413136insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17413136Submitted genomicNC_000004.12:g.109
217059_109217060in
s355
GRCh38 (hg38)NC_000004.12Chr4109,217,059109,217,059
nssv17413136RemappedPerfectNC_000004.11:g.110
138215_110138216in
s355
GRCh37.p13First PassNC_000004.11Chr4110,138,215110,138,215

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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