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nsv5463040

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:209

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 143 SVs from 34 studies. See in: genome view    
Submitted genomic68,242,203-68,242,411Question Mark
Overlapping variant regions from other studies: 143 SVs from 34 studies. See in: genome view    
Remapped(Score: Perfect):69,107,921-69,108,129Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5463040Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr468,242,20368,242,411
nsv5463040RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr469,107,92169,108,129

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16949549deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16949549Submitted genomicNC_000004.12:g.682
42203_68242411del
GRCh38 (hg38)NC_000004.12Chr468,242,20368,242,411
nssv16949549RemappedPerfectNC_000004.11:g.691
07921_69108129del
GRCh37.p13First PassNC_000004.11Chr469,107,92169,108,129

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)
nssv169495490.015906398
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