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nsv5439863

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:64

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 106 SVs from 23 studies. See in: genome view    
Submitted genomic102,109,359-102,109,422Question Mark
Overlapping variant regions from other studies: 106 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):102,725,819-102,725,882Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5439863Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2102,109,359102,109,422
nsv5439863RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2102,725,819102,725,882

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16916403deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16916403Submitted genomicNC_000002.12:g.102
109359_102109422de
l
GRCh38 (hg38)NC_000002.12Chr2102,109,359102,109,422
nssv16916403RemappedPerfectNC_000002.11:g.102
725819_102725882de
l
GRCh37.p13First PassNC_000002.11Chr2102,725,819102,725,882

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)
nssv169164030.01636404
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