nsv5478924

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:336

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 144 SVs from 49 studies. See in: genome view    
Submitted genomic106,093,547-106,093,882Question Mark
Overlapping variant regions from other studies: 144 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):105,733,993-105,734,328Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5478924Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7106,093,547106,093,882
nsv5478924RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7105,733,993105,734,328

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001604deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001604Submitted genomicNC_000007.14:g.106
093547_106093882de
l
GRCh38 (hg38)NC_000007.14Chr7106,093,547106,093,882
nssv17001604RemappedPerfectNC_000007.13:g.105
733993_105734328de
l
GRCh37.p13First PassNC_000007.13Chr7105,733,993105,734,328

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)
nssv170016040.32821036404
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