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nsv5536323

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:12,268

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 323 SVs from 53 studies. See in: genome view    
Submitted genomic21,907,467-21,919,734Question Mark
Overlapping variant regions from other studies: 323 SVs from 53 studies. See in: genome view    
Remapped(Score: Good):22,261,807-22,274,107Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5536323Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000022.11Chr2221,907,46721,919,734
nsv5536323RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000022.10Chr2222,261,80722,274,107

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17727826deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17727826Submitted genomicNC_000022.11:g.219
07467_21919734del
GRCh38 (hg38)NC_000022.11Chr2221,907,46721,919,734
nssv17727826RemappedGoodNC_000022.10:g.222
61807_22274107del
GRCh37.p13First PassNC_000022.10Chr2222,261,80722,274,107

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)
nssv17727826<0.00116404
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