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nsv5489101

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,454

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 123 SVs from 29 studies. See in: genome view    
Submitted genomic128,719,138-128,721,591Question Mark
Overlapping variant regions from other studies: 123 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):128,359,192-128,361,645Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489101Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7128,719,138128,721,591
nsv5489101RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7128,359,192128,361,645

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17002584deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17002584Submitted genomicNC_000007.14:g.128
719138_128721591de
l
GRCh38 (hg38)NC_000007.14Chr7128,719,138128,721,591
nssv17002584RemappedPerfectNC_000007.13:g.128
359192_128361645de
l
GRCh37.p13First PassNC_000007.13Chr7128,359,192128,361,645

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)
nssv17002584<0.00126404
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