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nsv5499035

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:207,090

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 2095 SVs from 103 studies. See in: genome view    
Submitted genomic7,853,043-8,060,132Question Mark
Overlapping variant regions from other studies: 2095 SVs from 103 studies. See in: genome view    
Remapped(Score: Perfect):8,005,639-8,212,728Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5499035Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr127,853,0438,060,132
nsv5499035RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr128,005,6398,212,728

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17054720duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17054720Submitted genomicNC_000012.12:g.785
3043_8060132dup
GRCh38 (hg38)NC_000012.12Chr127,853,0438,060,132
nssv17054720RemappedPerfectNC_000012.11:g.800
5639_8212728dup
GRCh37.p13First PassNC_000012.11Chr128,005,6398,212,728

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)
nssv170547200.004256394
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