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nsv5521878

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:15,913

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 244 SVs from 50 studies. See in: genome view    
Submitted genomic4,885,595-4,901,507Question Mark
Overlapping variant regions from other studies: 244 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):4,885,607-4,901,519Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5521878Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr194,885,5954,901,507
nsv5521878RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr194,885,6074,901,519

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17720784duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17720784Submitted genomicNC_000019.10:g.488
5595_4901507dup
GRCh38 (hg38)NC_000019.10Chr194,885,5954,901,507
nssv17720784RemappedPerfectNC_000019.9:g.4885
607_4901519dup
GRCh37.p13First PassNC_000019.9Chr194,885,6074,901,519

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)
nssv17720784<0.00146404
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