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nsv5424410

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 98 SVs from 24 studies. See in: genome view    
Submitted genomic33,080,387-33,080,460Question Mark
Overlapping variant regions from other studies: 98 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):33,545,988-33,546,061Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424410Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr133,080,38733,080,460
nsv5424410RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr133,545,98833,546,061

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901385deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901385Submitted genomicNC_000001.11:g.330
80387_33080460del
GRCh38 (hg38)NC_000001.11Chr133,080,38733,080,460
nssv16901385RemappedPerfectNC_000001.10:g.335
45988_33546061del
GRCh37.p13First PassNC_000001.10Chr133,545,98833,546,061

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)
nssv16901385<0.00116404
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