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nsv5563888

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 173 SVs from 22 studies. See in: genome view    
Submitted genomic155,395,892-155,395,943Question Mark
Overlapping variant regions from other studies: 173 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):155,188,587-155,188,638Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563888Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr7155,395,892155,395,943
nsv5563888RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr7155,188,587155,188,638

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17006847sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17006847Submitted genomicNC_000007.14:g.155
395892_155395943in
s897
GRCh38 (hg38)NC_000007.14Chr7155,395,892155,395,943
nssv17006847RemappedPerfectNC_000007.13:g.155
188587_155188638in
s897
GRCh37.p13First PassNC_000007.13Chr7155,188,587155,188,638

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)
nssv17006847<0.00116404
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