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nsv4853655

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:530

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 116 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):44,962,417-44,962,948Question Mark
Overlapping variant regions from other studies: 116 SVs from 24 studies. See in: genome view    
Submitted genomic43,591,058-43,591,589Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4853655RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr2044,962,417 (+36)44,962,946 (-43, +2)
nsv4853655Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000020.10Chr2043,591,058 (+36)43,591,587 (-43, +2)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16377121deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16377121RemappedPerfectNC_000020.11:g.(?_
44962453)_(4496290
3_44962948)del
GRCh38.p12First PassNC_000020.11Chr2044,962,417 (+36)44,962,946 (-43, +2)
nssv16377121Submitted genomicNC_000020.10:g.(?_
43591094)_(4359154
4_43591589)del
GRCh37 (hg19)NC_000020.10Chr2043,591,058 (+36)43,591,587 (-43, +2)

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)
nssv16377121<0.001116834
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