U.S. flag

An official website of the United States government

nsv5512307

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:221,521

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 711 SVs from 80 studies. See in: genome view    
Submitted genomic48,143,071-48,364,591Question Mark
Overlapping variant regions from other studies: 711 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):48,536,854-48,758,374Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5512307Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1248,143,07148,364,591
nsv5512307RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1248,536,85448,758,374

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056867duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056867Submitted genomicNC_000012.12:g.481
43071_48364591dup
GRCh38 (hg38)NC_000012.12Chr1248,143,07148,364,591
nssv17056867RemappedPerfectNC_000012.11:g.485
36854_48758374dup
GRCh37.p13First PassNC_000012.11Chr1248,536,85448,758,374

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)
nssv17056867<0.00146404
Support Center