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nsv5451647

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,880

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 24 studies. See in: genome view    
Submitted genomic231,053,807-231,055,686Question Mark
Overlapping variant regions from other studies: 92 SVs from 24 studies. See in: genome view    
Remapped(Score: Perfect):231,918,521-231,920,400Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5451647Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,053,807231,055,686
nsv5451647RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,918,521231,920,400

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928545deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928545Submitted genomicNC_000002.12:g.231
053807_231055686de
l
GRCh38 (hg38)NC_000002.12Chr2231,053,807231,055,686
nssv16928545RemappedPerfectNC_000002.11:g.231
918521_231920400de
l
GRCh37.p13First PassNC_000002.11Chr2231,918,521231,920,400

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)
nssv16928545<0.00126404
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