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nsv5480068

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,065

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 467 SVs from 50 studies. See in: genome view    
Submitted genomic144,492,623-144,495,687Question Mark
Overlapping variant regions from other studies: 466 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):145,718,006-145,721,070Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480068Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,492,623144,495,687
nsv5480068RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,718,006145,721,070

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17019337deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17019337Submitted genomicNC_000008.11:g.144
492623_144495687de
l
GRCh38 (hg38)NC_000008.11Chr8144,492,623144,495,687
nssv17019337RemappedPerfectNC_000008.10:g.145
718006_145721070de
l
GRCh37.p13First PassNC_000008.10Chr8145,718,006145,721,070

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)
nssv170193370.002136404
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