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nsv5437602

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:532,501

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1924 SVs from 101 studies. See in: genome view    
Submitted genomic131,208,309-131,740,809Question Mark
Overlapping variant regions from other studies: 1924 SVs from 101 studies. See in: genome view    
Remapped(Score: Perfect):131,965,882-132,498,382Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5437602Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,208,309131,740,809
nsv5437602RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2131,965,882132,498,382

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16919224duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16919224Submitted genomicNC_000002.12:g.131
208309_131740809du
p
GRCh38 (hg38)NC_000002.12Chr2131,208,309131,740,809
nssv16919224RemappedPerfectNC_000002.11:g.131
965882_132498382du
p
GRCh37.p13First PassNC_000002.11Chr2131,965,882132,498,382

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)
nssv16919224<0.00126390
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