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nsv5541060

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:45,906,595

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 11443 SVs from 66 studies. See in: genome view    
Submitted genomic10,926,699-56,833,293Question Mark
Overlapping variant regions from other studies: 11505 SVs from 70 studies. See in: genome view    
Remapped(Score: Good):13,193,955-58,979,440Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5541060Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000024.10ChrY10,926,69956,833,293
nsv5541060RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000024.9ChrY13,193,95558,979,440

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17738372insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17738372Submitted genomicNC_000024.10:g.109
26699_56833293ins5
1
GRCh38 (hg38)NC_000024.10ChrY10,926,69956,833,293
nssv17738372RemappedGoodNC_000024.9:g.1319
3955_58979440ins51
GRCh37.p13First PassNC_000024.9ChrY13,193,95558,979,440

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)
nssv177383720.48415493198
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