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nsv5449446

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:838

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 158 SVs from 32 studies. See in: genome view    
Submitted genomic61,881,422-61,882,259Question Mark
Overlapping variant regions from other studies: 158 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):62,108,557-62,109,394Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449446Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr261,881,42261,882,259
nsv5449446RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr262,108,55762,109,394

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16914505deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16914505Submitted genomicNC_000002.12:g.618
81422_61882259del
GRCh38 (hg38)NC_000002.12Chr261,881,42261,882,259
nssv16914505RemappedPerfectNC_000002.11:g.621
08557_62109394del
GRCh37.p13First PassNC_000002.11Chr262,108,55762,109,394

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)
nssv169145050.002106404
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