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nsv5457670

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:7,897

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 92 SVs from 28 studies. See in: genome view    
Submitted genomic39,056,766-39,064,662Question Mark
Overlapping variant regions from other studies: 92 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):39,056,868-39,064,764Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5457670Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr539,056,76639,064,662
nsv5457670RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr539,056,86839,064,764

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16964844deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16964844Submitted genomicNC_000005.10:g.390
56766_39064662del
GRCh38 (hg38)NC_000005.10Chr539,056,76639,064,662
nssv16964844RemappedPerfectNC_000005.9:g.3905
6868_39064764del
GRCh37.p13First PassNC_000005.9Chr539,056,86839,064,764

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)
nssv16964844<0.00116402
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