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nsv5432272

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:68,013

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1222 SVs from 77 studies. See in: genome view    
Submitted genomic1,455,988-1,524,000Question Mark
Overlapping variant regions from other studies: 1222 SVs from 77 studies. See in: genome view    
Remapped(Score: Perfect):1,391,368-1,459,380Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5432272Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr11,455,9881,524,000
nsv5432272RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr11,391,3681,459,380

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16900989deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16900989Submitted genomicNC_000001.11:g.145
5988_1524000del
GRCh38 (hg38)NC_000001.11Chr11,455,9881,524,000
nssv16900989RemappedPerfectNC_000001.10:g.139
1368_1459380del
GRCh37.p13First PassNC_000001.10Chr11,391,3681,459,380

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)
nssv16900989<0.00125934
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