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nsv6147428

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:8,652

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 160 SVs from 25 studies. See in: genome view    
Submitted genomic93,480,404-93,489,055Question Mark
Overlapping variant regions from other studies: 160 SVs from 25 studies. See in: genome view    
Remapped(Score: Perfect):94,492,632-94,501,283Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6147428Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr893,480,40493,489,055
nsv6147428RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr894,492,63294,501,283

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17014483mobile element deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17014483Submitted genomicNC_000008.11:g.934
80404_93489055del
GRCh38 (hg38)NC_000008.11Chr893,480,40493,489,055
nssv17014483RemappedPerfectNC_000008.10:g.944
92632_94501283del
GRCh37.p13First PassNC_000008.10Chr894,492,63294,501,283

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)
nssv17014483<0.00126404
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