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nsv5520806

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:900,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2892 SVs from 96 studies. See in: genome view    
Submitted genomic9,332,000-10,232,000Question Mark
Overlapping variant regions from other studies: 2892 SVs from 96 studies. See in: genome view    
Remapped(Score: Perfect):9,331,998-10,231,997Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520806Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr189,332,00010,232,000
nsv5520806RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr189,331,99810,231,997

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17715309deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17715309Submitted genomicNC_000018.10:g.933
2000_10232000del
GRCh38 (hg38)NC_000018.10Chr189,332,00010,232,000
nssv17715309RemappedPerfectNC_000018.9:g.9331
998_10231997del
GRCh37.p13First PassNC_000018.9Chr189,331,99810,231,997

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)
nssv17715309<0.00116404
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