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nsv5442321

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:691,399

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1650 SVs from 76 studies. See in: genome view    
Submitted genomic115,970,005-116,661,403Question Mark
Overlapping variant regions from other studies: 1650 SVs from 76 studies. See in: genome view    
Remapped(Score: Perfect):116,727,581-117,418,979Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5442321Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2115,970,005116,661,403
nsv5442321RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2116,727,581117,418,979

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16918001deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16918001Submitted genomicNC_000002.12:g.115
970005_116661403de
l
GRCh38 (hg38)NC_000002.12Chr2115,970,005116,661,403
nssv16918001RemappedPerfectNC_000002.11:g.116
727581_117418979de
l
GRCh37.p13First PassNC_000002.11Chr2116,727,581117,418,979

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)
nssv16918001<0.00116404
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