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nsv5457825

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,414

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 212 SVs from 39 studies. See in: genome view    
Submitted genomic167,129,527-167,130,940Question Mark
Overlapping variant regions from other studies: 212 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):167,543,015-167,544,428Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457825Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6167,129,527167,130,940
nsv5457825RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6167,543,015167,544,428

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16991254deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16991254Submitted genomicNC_000006.12:g.167
129527_167130940de
l
GRCh38 (hg38)NC_000006.12Chr6167,129,527167,130,940
nssv16991254RemappedPerfectNC_000006.11:g.167
543015_167544428de
l
GRCh37.p13First PassNC_000006.11Chr6167,543,015167,544,428

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)
nssv169912540.0221386404
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