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nsv5487987

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:61

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 genomic128,751,156-128,751,216Question Mark
Overlapping variant regions from other studies: 123 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):128,391,210-128,391,270Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487987Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7128,751,156128,751,216
nsv5487987RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7128,391,210128,391,270

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17002586deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17002586Submitted genomicNC_000007.14:g.128
751156_128751216de
l
GRCh38 (hg38)NC_000007.14Chr7128,751,156128,751,216
nssv17002586RemappedPerfectNC_000007.13:g.128
391210_128391270de
l
GRCh37.p13First PassNC_000007.13Chr7128,391,210128,391,270

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)
nssv17002586<0.00166404
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