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nsv5531475

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:55

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 132 SVs from 16 studies. See in: genome view    
Submitted genomic61,482,671-61,482,725Question Mark
Overlapping variant regions from other studies: 132 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):59,560,032-59,560,086Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531475Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1761,482,67161,482,725
nsv5531475RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1759,560,03259,560,086

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724961duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724961Submitted genomicNC_000017.11:g.614
82671_61482725dup
GRCh38 (hg38)NC_000017.11Chr1761,482,67161,482,725
nssv17724961RemappedPerfectNC_000017.10:g.595
60032_59560086dup
GRCh37.p13First PassNC_000017.10Chr1759,560,03259,560,086

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)
nssv17724961<0.00126404
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