U.S. flag

An official website of the United States government

nsv5460832

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:18,420

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 181 SVs from 37 studies. See in: genome view    
Submitted genomic67,415,404-67,433,823Question Mark
Overlapping variant regions from other studies: 181 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):68,281,122-68,299,541Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5460832Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr467,415,40467,433,823
nsv5460832RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr468,281,12268,299,541

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16949483duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16949483Submitted genomicNC_000004.12:g.674
15404_67433823dup
GRCh38 (hg38)NC_000004.12Chr467,415,40467,433,823
nssv16949483RemappedPerfectNC_000004.11:g.682
81122_68299541dup
GRCh37.p13First PassNC_000004.11Chr468,281,12268,299,541

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)
nssv16949483<0.00156404
Support Center