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nsv4972871

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,809

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 129 SVs from 35 studies. See in: genome view    
Submitted genomic56,263,974-56,267,783Question Mark
Overlapping variant regions from other studies: 129 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):56,657,758-56,661,567Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4972871Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1256,263,975 (-1, +1)56,267,783 (-1)
nsv4972871RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,657,759 (-1, +1)56,661,567 (-1)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16537296deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16537296Submitted genomicNC_000012.12:g.(56
263974_56263976)_(
56267782_?)del
GRCh38 (hg38)NC_000012.12Chr1256,263,975 (-1, +1)56,267,783 (-1)
nssv16537296RemappedPerfectNC_000012.11:g.(56
657758_56657760)_(
56661566_?)del
GRCh37.p13First PassNC_000012.11Chr1256,657,759 (-1, +1)56,661,567 (-1)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16537296<0.001129246
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