U.S. flag

An official website of the United States government

nsv5447555

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,464

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 181 SVs from 55 studies. See in: genome view    
Submitted genomic212,297,811-212,299,274Question Mark
Overlapping variant regions from other studies: 185 SVs from 55 studies. See in: genome view    
Remapped(Score: Perfect):212,471,153-212,472,616Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5447555Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1212,297,811212,299,274
nsv5447555RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1212,471,153212,472,616

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16896093deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16896093Submitted genomicNC_000001.11:g.212
297811_212299274de
l
GRCh38 (hg38)NC_000001.11Chr1212,297,811212,299,274
nssv16896093RemappedPerfectNC_000001.10:g.212
471153_212472616de
l
GRCh37.p13First PassNC_000001.10Chr1212,471,153212,472,616

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)
nssv168960930.67343106402
Support Center