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nsv5458635

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 23 studies. See in: genome view    
Submitted genomic13,587,089-13,587,169Question Mark
Overlapping variant regions from other studies: 120 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):13,587,321-13,587,401Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5458635Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr613,587,08913,587,169
nsv5458635RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr613,587,32113,587,401

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16979684deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16979684Submitted genomicNC_000006.12:g.135
87089_13587169del
GRCh38 (hg38)NC_000006.12Chr613,587,08913,587,169
nssv16979684RemappedPerfectNC_000006.11:g.135
87321_13587401del
GRCh37.p13First PassNC_000006.11Chr613,587,32113,587,401

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)
nssv169796840.0211366404
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