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nsv5458755

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,162

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 97 SVs from 27 studies. See in: genome view    
Submitted genomic153,101,122-153,105,283Question Mark
Overlapping variant regions from other studies: 97 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):153,422,257-153,426,418Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5458755Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr6153,101,122153,105,283
nsv5458755RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr6153,422,257153,426,418

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16989084duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16989084Submitted genomicNC_000006.12:g.153
101122_153105283du
p
GRCh38 (hg38)NC_000006.12Chr6153,101,122153,105,283
nssv16989084RemappedPerfectNC_000006.11:g.153
422257_153426418du
p
GRCh37.p13First PassNC_000006.11Chr6153,422,257153,426,418

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)
nssv16989084<0.00136404
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