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nsv6052484

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 119 SVs from 22 studies. See in: genome view    
Submitted genomic207,048,650-207,048,650Question Mark
Overlapping variant regions from other studies: 125 SVs from 22 studies. See in: genome view    
Remapped(Score: Perfect):207,221,995-207,221,995Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6052484Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1207,048,650207,048,650
nsv6052484RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1207,221,995207,221,995

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17525087insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17525087Submitted genomicNC_000001.11:g.207
048650_207048651in
s102
GRCh38 (hg38)NC_000001.11Chr1207,048,650207,048,650
nssv17525087RemappedPerfectNC_000001.10:g.207
221995_207221996in
s102
GRCh37.p13First PassNC_000001.10Chr1207,221,995207,221,995

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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