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nsv4573285

  • 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: 33 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):45,514,651-45,514,651Question Mark
Overlapping variant regions from other studies: 33 SVs from 6 studies. See in: genome view    
Submitted genomic45,980,323-45,980,323Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4573285RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000001.11Chr145,514,65145,514,651
nsv4573285Submitted genomicGRCh37.p13Primary AssemblyNC_000001.10Chr145,980,32345,980,323

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16024654sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16024654RemappedPerfectNC_000001.11:g.455
14651_45514652ins2
68
GRCh38.p12First PassNC_000001.11Chr145,514,65145,514,651
nssv16024654Submitted genomicNC_000001.10:g.459
80323_45980324ins2
68
GRCh37.p13NC_000001.10Chr145,980,32345,980,323

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv160246544.6e-005121694
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