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nsv5490706

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:124,155

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 314 SVs from 52 studies. See in: genome view    
Submitted genomic56,275,910-56,400,064Question Mark
Overlapping variant regions from other studies: 314 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):58,035,671-58,159,825Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5490706Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1056,275,91056,400,064
nsv5490706RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1058,035,67158,159,825

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17032913duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17032913Submitted genomicNC_000010.11:g.562
75910_56400064dup
GRCh38 (hg38)NC_000010.11Chr1056,275,91056,400,064
nssv17032913RemappedPerfectNC_000010.10:g.580
35671_58159825dup
GRCh37.p13First PassNC_000010.10Chr1058,035,67158,159,825

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)
nssv17032913<0.00126404
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