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nsv5487809

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:9,455

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 26 studies. See in: genome view    
Submitted genomic117,660,797-117,670,251Question Mark
Overlapping variant regions from other studies: 151 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):117,300,851-117,310,305Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5487809Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7117,660,797117,670,251
nsv5487809RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7117,300,851117,310,305

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17001707deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17001707Submitted genomicNC_000007.14:g.117
660797_117670251de
l
GRCh38 (hg38)NC_000007.14Chr7117,660,797117,670,251
nssv17001707RemappedPerfectNC_000007.13:g.117
300851_117310305de
l
GRCh37.p13First PassNC_000007.13Chr7117,300,851117,310,305

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)
nssv17001707<0.00116404
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