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nsv5520330

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,866,512

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 5689 SVs from 116 studies. See in: genome view    
Submitted genomic14,022,600-15,889,111Question Mark
Overlapping variant regions from other studies: 5689 SVs from 116 studies. See in: genome view    
Remapped(Score: Perfect):13,925,917-15,792,425Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520330Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1714,022,60015,889,111
nsv5520330RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1713,925,91715,792,425

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17711592deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17711592Submitted genomicNC_000017.11:g.140
22600_15889111del
GRCh38 (hg38)NC_000017.11Chr1714,022,60015,889,111
nssv17711592RemappedPerfectNC_000017.10:g.139
25917_15792425del
GRCh37.p13First PassNC_000017.10Chr1713,925,91715,792,425

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)
nssv17711592<0.00116404
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