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nsv5522435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,257

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 30 studies. See in: genome view    
Submitted genomic17,990,565-18,002,821Question Mark
Overlapping variant regions from other studies: 132 SVs from 30 studies. See in: genome view    
Remapped(Score: Perfect):18,101,374-18,113,630Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5522435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1917,990,56518,002,821
nsv5522435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1918,101,37418,113,630

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17721992deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17721992Submitted genomicNC_000019.10:g.179
90565_18002821del
GRCh38 (hg38)NC_000019.10Chr1917,990,56518,002,821
nssv17721992RemappedPerfectNC_000019.9:g.1810
1374_18113630del
GRCh37.p13First PassNC_000019.9Chr1918,101,37418,113,630

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)
nssv17721992<0.00116404
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