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nsv5479229

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:132,279

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 937 SVs from 88 studies. See in: genome view    
Submitted genomic144,946,222-145,078,500Question Mark
Overlapping variant regions from other studies: 938 SVs from 88 studies. See in: genome view    
Remapped(Score: Perfect):146,171,608-146,303,886Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5479229Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,946,222145,078,500
nsv5479229RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8146,171,608146,303,886

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17019414duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17019414Submitted genomicNC_000008.11:g.144
946222_145078500du
p
GRCh38 (hg38)NC_000008.11Chr8144,946,222145,078,500
nssv17019414RemappedPerfectNC_000008.10:g.146
171608_146303886du
p
GRCh37.p13First PassNC_000008.10Chr8146,171,608146,303,886

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)
nssv17019414<0.00166404
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