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nsv5469336

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:387

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 151 SVs from 31 studies. See in: genome view    
Submitted genomic95,504,262-95,504,648Question Mark
Overlapping variant regions from other studies: 151 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):94,839,966-94,840,352Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5469336Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr595,504,26295,504,648
nsv5469336RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr594,839,96694,840,352

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16972394deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16972394Submitted genomicNC_000005.10:g.955
04262_95504648del
GRCh38 (hg38)NC_000005.10Chr595,504,26295,504,648
nssv16972394RemappedPerfectNC_000005.9:g.9483
9966_94840352del
GRCh37.p13First PassNC_000005.9Chr594,839,96694,840,352

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)
nssv169723940.012756404
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