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nsv5483435

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,107

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 465 SVs from 50 studies. See in: genome view    
Submitted genomic144,494,577-144,495,683Question Mark
Overlapping variant regions from other studies: 464 SVs from 50 studies. See in: genome view    
Remapped(Score: Perfect):145,719,960-145,721,066Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5483435Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8144,494,577144,495,683
nsv5483435RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr8145,719,960145,721,066

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17019338deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17019338Submitted genomicNC_000008.11:g.144
494577_144495683de
l
GRCh38 (hg38)NC_000008.11Chr8144,494,577144,495,683
nssv17019338RemappedPerfectNC_000008.10:g.145
719960_145721066de
l
GRCh37.p13First PassNC_000008.10Chr8145,719,960145,721,066

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)
nssv17019338<0.00116404
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