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nsv5868120

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,088

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 193 SVs from 34 studies. See in: genome view    
Submitted genomic190,356,913-190,358,000Question Mark
Overlapping variant regions from other studies: 193 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):190,326,043-190,327,130Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5868120Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1190,356,913190,358,000
nsv5868120RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1190,326,043190,327,130

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17362774deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17362774Submitted genomicNC_000001.11:g.190
356913_190358000de
l
GRCh38 (hg38)NC_000001.11Chr1190,356,913190,358,000
nssv17362774RemappedPerfectNC_000001.10:g.190
326043_190327130de
l
GRCh37.p13First PassNC_000001.10Chr1190,326,043190,327,130

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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