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nsv5525434

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:96

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
Submitted genomic43,895,260-43,895,355Question Mark
Overlapping variant regions from other studies: 91 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):44,399,412-44,399,507Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525434Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1943,895,26043,895,355
nsv5525434RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1944,399,41244,399,507

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17725209deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17725209Submitted genomicNC_000019.10:g.438
95260_43895355del
GRCh38 (hg38)NC_000019.10Chr1943,895,26043,895,355
nssv17725209RemappedPerfectNC_000019.9:g.4439
9412_44399507del
GRCh37.p13First PassNC_000019.9Chr1944,399,41244,399,507

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)
nssv17725209<0.00156404
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