U.S. flag

An official website of the United States government

nsv5452929

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 94 SVs from 26 studies. See in: genome view    
Submitted genomic48,668,735-48,668,808Question Mark
Overlapping variant regions from other studies: 94 SVs from 26 studies. See in: genome view    
Remapped(Score: Perfect):48,706,168-48,706,241Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5452929Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000003.12Chr348,668,73548,668,808
nsv5452929RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000003.11Chr348,706,16848,706,241

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16933752deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16933752Submitted genomicNC_000003.12:g.486
68735_48668808del
GRCh38 (hg38)NC_000003.12Chr348,668,73548,668,808
nssv16933752RemappedPerfectNC_000003.11:g.487
06168_48706241del
GRCh37.p13First PassNC_000003.11Chr348,706,16848,706,241

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)
nssv16933752<0.00126404
Support Center