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nsv5499565

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
Submitted genomic47,877,047-47,877,110Question Mark
Overlapping variant regions from other studies: 79 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):48,270,830-48,270,893Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499565Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1247,877,04747,877,110
nsv5499565RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1248,270,83048,270,893

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056850duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056850Submitted genomicNC_000012.12:g.478
77047_47877110dup
GRCh38 (hg38)NC_000012.12Chr1247,877,04747,877,110
nssv17056850RemappedPerfectNC_000012.11:g.482
70830_48270893dup
GRCh37.p13First PassNC_000012.11Chr1248,270,83048,270,893

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)
nssv17056850<0.00116404
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