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nsv5555698

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:13

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 89 SVs from 20 studies. See in: genome view    
Submitted genomic32,081,269-32,081,281Question Mark
Overlapping variant regions from other studies: 89 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):32,550,475-32,550,487Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5555698Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1432,081,26932,081,281
nsv5555698RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1432,550,47532,550,487

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17693580line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17693580Submitted genomicNC_000014.9:g.3208
1269_32081281ins60
19
GRCh38 (hg38)NC_000014.9Chr1432,081,26932,081,281
nssv17693580RemappedPerfectNC_000014.8:g.3255
0475_32550487ins60
19
GRCh37.p13First PassNC_000014.8Chr1432,550,47532,550,487

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)
nssv17693580<0.00116404
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