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nsv5448639

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:525

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 88 SVs from 18 studies. See in: genome view    
Submitted genomic231,088,055-231,088,579Question Mark
Overlapping variant regions from other studies: 88 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):231,952,769-231,953,293Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5448639Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2231,088,055231,088,579
nsv5448639RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2231,952,769231,953,293

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16928549duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16928549Submitted genomicNC_000002.12:g.231
088055_231088579du
p
GRCh38 (hg38)NC_000002.12Chr2231,088,055231,088,579
nssv16928549RemappedPerfectNC_000002.11:g.231
952769_231953293du
p
GRCh37.p13First PassNC_000002.11Chr2231,952,769231,953,293

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)
nssv16928549<0.00136404
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