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nsv5465294

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:65

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 17 studies. See in: genome view    
Submitted genomic143,814,572-143,814,636Question Mark
Overlapping variant regions from other studies: 88 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):144,135,709-144,135,773Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465294Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6143,814,572143,814,636
nsv5465294RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6144,135,709144,135,773

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16971235duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16971235Submitted genomicNC_000006.12:g.143
814572_143814636du
p
GRCh38 (hg38)NC_000006.12Chr6143,814,572143,814,636
nssv16971235RemappedPerfectNC_000006.11:g.144
135709_144135773du
p
GRCh37.p13First PassNC_000006.11Chr6144,135,709144,135,773

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)
nssv169712350.01636404
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