U.S. flag

An official website of the United States government

nsv5466612

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:82,913

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 312 SVs from 52 studies. See in: genome view    
Submitted genomic13,524,856-13,607,768Question Mark
Overlapping variant regions from other studies: 312 SVs from 52 studies. See in: genome view    
Remapped(Score: Perfect):13,525,088-13,608,000Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5466612Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000006.12Chr613,524,85613,607,768
nsv5466612RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000006.11Chr613,525,08813,608,000

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16979680deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16979680Submitted genomicNC_000006.12:g.135
24856_13607768del
GRCh38 (hg38)NC_000006.12Chr613,524,85613,607,768
nssv16979680RemappedPerfectNC_000006.11:g.135
25088_13608000del
GRCh37.p13First PassNC_000006.11Chr613,525,08813,608,000

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)
nssv16979680<0.00116404
Support Center