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nsv5436981

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:135

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 99 SVs from 18 studies. See in: genome view    
Submitted genomic170,378,416-170,378,550Question Mark
Overlapping variant regions from other studies: 99 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):170,096,204-170,096,338Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5436981Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr3170,378,416170,378,550
nsv5436981RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr3170,096,204170,096,338

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16943427duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16943427Submitted genomicNC_000003.12:g.170
378416_170378550du
p
GRCh38 (hg38)NC_000003.12Chr3170,378,416170,378,550
nssv16943427RemappedPerfectNC_000003.11:g.170
096204_170096338du
p
GRCh37.p13First PassNC_000003.11Chr3170,096,204170,096,338

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)
nssv16943427<0.00136404
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