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nsv4523070

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,011,004

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 761 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):57,950,170-58,961,173Question Mark
Overlapping variant regions from other studies: 761 SVs from 20 studies. See in: genome view    
Submitted genomic57,245,997-58,257,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4523070RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000005.10Chr557,950,17058,961,173
nsv4523070Submitted genomicGRCh37.p13Primary AssemblyNC_000005.9Chr557,245,99758,257,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15976370duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15976370RemappedPerfectNC_000005.10:g.579
50170_58961173dup
GRCh38.p12First PassNC_000005.10Chr557,950,17058,961,173
nssv15976370Submitted genomicNC_000005.9:g.5724
5997_58257000dup
GRCh37.p13NC_000005.9Chr557,245,99758,257,000

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)
nssv159763704.6e-005121694
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