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nsv5489204

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:78

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 72 SVs from 19 studies. See in: genome view    
Submitted genomic43,401,091-43,401,168Question Mark
Overlapping variant regions from other studies: 68 SVs from 16 studies. See in: genome view    
Remapped(Score: Perfect):43,896,539-43,896,616Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5489204Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1043,401,09143,401,168
nsv5489204RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1043,896,53943,896,616

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17032758deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17032758Submitted genomicNC_000010.11:g.434
01091_43401168del
GRCh38 (hg38)NC_000010.11Chr1043,401,09143,401,168
nssv17032758RemappedPerfectNC_000010.10:g.438
96539_43896616del
GRCh37.p13First PassNC_000010.10Chr1043,896,53943,896,616

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)
nssv17032758<0.00166404
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