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nsv5423357

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,177

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 137 SVs from 33 studies. See in: genome view    
Submitted genomic32,082,586-32,087,762Question Mark
Overlapping variant regions from other studies: 137 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):32,548,187-32,553,363Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5423357Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr132,082,58632,087,762
nsv5423357RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr132,548,18732,553,363

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16901362deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16901362Submitted genomicNC_000001.11:g.320
82586_32087762del
GRCh38 (hg38)NC_000001.11Chr132,082,58632,087,762
nssv16901362RemappedPerfectNC_000001.10:g.325
48187_32553363del
GRCh37.p13First PassNC_000001.10Chr132,548,18732,553,363

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)
nssv16901362<0.00156404
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