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nsv5446307

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:397,394

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1191 SVs from 85 studies. See in: genome view    
Submitted genomic131,610,398-132,007,791Question Mark
Overlapping variant regions from other studies: 1191 SVs from 85 studies. See in: genome view    
Remapped(Score: Perfect):132,367,971-132,765,364Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5446307Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2131,610,398132,007,791
nsv5446307RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2132,367,971132,765,364

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16917846duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16917846Submitted genomicNC_000002.12:g.131
610398_132007791du
p
GRCh38 (hg38)NC_000002.12Chr2131,610,398132,007,791
nssv16917846RemappedPerfectNC_000002.11:g.132
367971_132765364du
p
GRCh37.p13First PassNC_000002.11Chr2132,367,971132,765,364

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)
nssv16917846<0.00126404
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