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nsv5449293

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:58

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 293 SVs from 33 studies. See in: genome view    
Submitted genomic240,542,866-240,542,923Question Mark
Overlapping variant regions from other studies: 293 SVs from 33 studies. See in: genome view    
Remapped(Score: Perfect):241,482,283-241,482,340Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5449293Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2240,542,866240,542,923
nsv5449293RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2241,482,283241,482,340

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16926504duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16926504Submitted genomicNC_000002.12:g.240
542866_240542923du
p
GRCh38 (hg38)NC_000002.12Chr2240,542,866240,542,923
nssv16926504RemappedPerfectNC_000002.11:g.241
482283_241482340du
p
GRCh37.p13First PassNC_000002.11Chr2241,482,283241,482,340

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)
nssv16926504<0.00116404
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