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nsv5480819

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:126

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
Submitted genomic4,654,783-4,654,908Question Mark
Overlapping variant regions from other studies: 120 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):4,696,975-4,697,100Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5480819Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr104,654,7834,654,908
nsv5480819RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr104,696,9754,697,100

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17029511deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17029511Submitted genomicNC_000010.11:g.465
4783_4654908del
GRCh38 (hg38)NC_000010.11Chr104,654,7834,654,908
nssv17029511RemappedPerfectNC_000010.10:g.469
6975_4697100del
GRCh37.p13First PassNC_000010.10Chr104,696,9754,697,100

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)
nssv17029511<0.00146404
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