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nsv5533377

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:117,091

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 497 SVs from 59 studies. See in: genome view    
Submitted genomic63,906,475-64,023,565Question Mark
Overlapping variant regions from other studies: 497 SVs from 59 studies. See in: genome view    
Remapped(Score: Perfect):61,983,835-62,100,925Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5533377Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1763,906,47564,023,565
nsv5533377RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1761,983,83562,100,925

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714038duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714038Submitted genomicNC_000017.11:g.639
06475_64023565dup
GRCh38 (hg38)NC_000017.11Chr1763,906,47564,023,565
nssv17714038RemappedPerfectNC_000017.10:g.619
83835_62100925dup
GRCh37.p13First PassNC_000017.10Chr1761,983,83562,100,925

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)
nssv17714038<0.00126404
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