U.S. flag

An official website of the United States government

nsv5498546

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,124

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 180 SVs from 43 studies. See in: genome view    
Submitted genomic12,505,914-12,520,037Question Mark
Overlapping variant regions from other studies: 181 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):12,658,848-12,672,971Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5498546Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1212,505,91412,520,037
nsv5498546RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1212,658,84812,672,971

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17053181deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17053181Submitted genomicNC_000012.12:g.125
05914_12520037del
GRCh38 (hg38)NC_000012.12Chr1212,505,91412,520,037
nssv17053181RemappedPerfectNC_000012.11:g.126
58848_12672971del
GRCh37.p13First PassNC_000012.11Chr1212,658,84812,672,971

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)
nssv17053181<0.00116404
Support Center