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nsv5445147

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:795,151

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2041 SVs from 79 studies. See in: genome view    
Submitted genomic230,482,037-231,277,187Question Mark
Overlapping variant regions from other studies: 2044 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):230,617,783-231,412,933Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5445147Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1230,482,037231,277,187
nsv5445147RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1230,617,783231,412,933

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896868duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896868Submitted genomicNC_000001.11:g.230
482037_231277187du
p
GRCh38 (hg38)NC_000001.11Chr1230,482,037231,277,187
nssv16896868RemappedPerfectNC_000001.10:g.230
617783_231412933du
p
GRCh37.p13First PassNC_000001.10Chr1230,617,783231,412,933

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)
nssv16896868<0.00116404
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