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nsv5893680

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,366

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 153 SVs from 32 studies. See in: genome view    
Submitted genomic109,687,389-109,693,754Question Mark
Overlapping variant regions from other studies: 153 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):110,008,592-110,014,957Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5893680Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6109,687,389109,693,754
nsv5893680RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6110,008,592110,014,957

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17415233deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17415233Submitted genomicNC_000006.12:g.109
687389_109693754de
l
GRCh38 (hg38)NC_000006.12Chr6109,687,389109,693,754
nssv17415233RemappedPerfectNC_000006.11:g.110
008592_110014957de
l
GRCh37.p13First PassNC_000006.11Chr6110,008,592110,014,957

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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