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nsv5520548

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,299

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 235 SVs from 41 studies. See in: genome view    
Submitted genomic52,289,775-52,335,073Question Mark
Overlapping variant regions from other studies: 235 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):52,793,028-52,838,326Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5520548Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1952,289,77552,335,073
nsv5520548RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1952,793,02852,838,326

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17724158duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17724158Submitted genomicNC_000019.10:g.522
89775_52335073dup
GRCh38 (hg38)NC_000019.10Chr1952,289,77552,335,073
nssv17724158RemappedPerfectNC_000019.9:g.5279
3028_52838326dup
GRCh37.p13First PassNC_000019.9Chr1952,793,02852,838,326

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)
nssv17724158<0.00116404
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