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nsv5525859

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,575

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 185 SVs from 46 studies. See in: genome view    
Submitted genomic46,119,481-46,125,055Question Mark
Overlapping variant regions from other studies: 185 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):46,622,738-46,628,312Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525859Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1946,119,48146,125,055
nsv5525859RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1946,622,73846,628,312

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723628deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723628Submitted genomicNC_000019.10:g.461
19481_46125055del
GRCh38 (hg38)NC_000019.10Chr1946,119,48146,125,055
nssv17723628RemappedPerfectNC_000019.9:g.4662
2738_46628312del
GRCh37.p13First PassNC_000019.9Chr1946,622,73846,628,312

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)
nssv177236280.0543446396
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