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nsv5449624

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:228

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 147 SVs from 23 studies. See in: genome view    
Submitted genomic231,162,136-231,162,363Question Mark
Overlapping variant regions from other studies: 150 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):231,297,882-231,298,109Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449624Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1231,162,136231,162,363
nsv5449624RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1231,297,882231,298,109

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896929deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896929Submitted genomicNC_000001.11:g.231
162136_231162363de
l
GRCh38 (hg38)NC_000001.11Chr1231,162,136231,162,363
nssv16896929RemappedPerfectNC_000001.10:g.231
297882_231298109de
l
GRCh37.p13First PassNC_000001.10Chr1231,297,882231,298,109

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)
nssv16896929<0.00126404
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