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nsv4798927

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,275

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 131 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):184,697,863-184,710,137Question Mark
Overlapping variant regions from other studies: 131 SVs from 29 studies. See in: genome view    
Submitted genomic184,415,651-184,427,925Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4798927RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000003.12Chr3184,697,863184,710,137
nsv4798927Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000003.11Chr3184,415,651184,427,925

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16319418deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16319418RemappedPerfectNC_000003.12:g.184
697863_184710137de
l
GRCh38.p12First PassNC_000003.12Chr3184,697,863184,710,137
nssv16319418Submitted genomicNC_000003.11:g.184
415651_184427925de
l
GRCh37 (hg19)NC_000003.11Chr3184,415,651184,427,925

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)
nssv16319418<0.001116834
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