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nsv5484232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,746

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 115 SVs from 25 studies. See in: genome view    
Submitted genomic138,828,198-138,830,943Question Mark
Overlapping variant regions from other studies: 115 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):138,512,943-138,515,688Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5484232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7138,828,198138,830,943
nsv5484232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7138,512,943138,515,688

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17006311deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17006311Submitted genomicNC_000007.14:g.138
828198_138830943de
l
GRCh38 (hg38)NC_000007.14Chr7138,828,198138,830,943
nssv17006311RemappedPerfectNC_000007.13:g.138
512943_138515688de
l
GRCh37.p13First PassNC_000007.13Chr7138,512,943138,515,688

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)
nssv17006311<0.00126404
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