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nsv5485252

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:379

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 81 SVs from 23 studies. See in: genome view    
Submitted genomic31,503,724-31,504,102Question Mark
Overlapping variant regions from other studies: 81 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):31,792,652-31,793,030Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485252Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1031,503,72431,504,102
nsv5485252RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1031,792,65231,793,030

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17031432deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17031432Submitted genomicNC_000010.11:g.315
03724_31504102del
GRCh38 (hg38)NC_000010.11Chr1031,503,72431,504,102
nssv17031432RemappedPerfectNC_000010.10:g.317
92652_31793030del
GRCh37.p13First PassNC_000010.10Chr1031,792,65231,793,030

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)
nssv17031432<0.00146404
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