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nsv5520269

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:87

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 103 SVs from 15 studies. See in: genome view    
Submitted genomic46,726,549-46,726,635Question Mark
Overlapping variant regions from other studies: 103 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):45,355,188-45,355,274Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520269Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000020.11Chr2046,726,54946,726,635
nsv5520269RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr2045,355,18845,355,274

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17732689duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17732689Submitted genomicNC_000020.11:g.467
26549_46726635dup
GRCh38 (hg38)NC_000020.11Chr2046,726,54946,726,635
nssv17732689RemappedPerfectNC_000020.10:g.453
55188_45355274dup
GRCh37.p13First PassNC_000020.10Chr2045,355,18845,355,274

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)
nssv17732689<0.00136404
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