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nsv5482885

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:151

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 19 studies. See in: genome view    
Submitted genomic48,917,593-48,917,743Question Mark
Overlapping variant regions from other studies: 103 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):49,830,152-49,830,302Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5482885Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr848,917,59348,917,743
nsv5482885RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr849,830,15249,830,302

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17010907deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17010907Submitted genomicNC_000008.11:g.489
17593_48917743del
GRCh38 (hg38)NC_000008.11Chr848,917,59348,917,743
nssv17010907RemappedPerfectNC_000008.10:g.498
30152_49830302del
GRCh37.p13First PassNC_000008.10Chr849,830,15249,830,302

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)
nssv17010907<0.00126404
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