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nsv5477528

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,127,881

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 3899 SVs from 99 studies. See in: genome view    
Submitted genomic55,282,120-56,410,000Question Mark
Overlapping variant regions from other studies: 3899 SVs from 99 studies. See in: genome view    
Remapped(Score: Perfect):55,349,813-56,477,693Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5477528Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000007.14Chr755,282,12056,410,000
nsv5477528RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000007.13Chr755,349,81356,477,693

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16997548duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16997548Submitted genomicNC_000007.14:g.552
82120_56410000dup
GRCh38 (hg38)NC_000007.14Chr755,282,12056,410,000
nssv16997548RemappedPerfectNC_000007.13:g.553
49813_56477693dup
GRCh37.p13First PassNC_000007.13Chr755,349,81356,477,693

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)
nssv16997548<0.00126404
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